| geneid | 960 |
|---|---|
| ensemblid | ENSG00000026508.21 |
| hgncid | 1681 |
| symbol | CD44 |
| name | CD44 molecule (Indian blood group) |
| refseq_nuc | NM_000610.4 |
| refseq_prot | NP_000601.3 |
| ensembl_nuc | ENST00000428726.8 |
| ensembl_prot | ENSP00000398632.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 35139171 |
| end | 35232402 |
| strand | + |
| ver | v1.2 |
| region | chr11:35139171-35232402 |
| region5000 | chr11:35134171-35237402 |
| regionname0 | CD44_chr11_35139171_35232402 |
| regionname5000 | CD44_chr11_35134171_35237402 |
| 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 | 0/1 | 742 | 321 | 79 | 44 | 160 | 7 | 30 | 123 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002 | 0/0 | 742 | 37 | 7 | 17 | 9 | 1 | 3 | 6 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0003 | 1/0 | 742 | 9 | 0 | 7 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0004 | 0/0 | 742 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0005 | 0/0 | 742 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0006 | 0/0 | 742 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0007 | 0/0 | 742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0008 | 0/0 | 56 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2229 | 254 | 38 | 32 | 149 | 7 | 27 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0002 | 0/0 | 2229 | 25 | 24 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0003 | 0/0 | 2229 | 22 | 6 | 9 | 4 | 1 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0004 | 0/0 | 2229 | 21 | 5 | 6 | 8 | 0 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0005 | 0/0 | 2229 | 15 | 1 | 8 | 5 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0006 | 1/0 | 2229 | 8 | 0 | 6 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0007 | 0/0 | 2229 | 8 | 7 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0008 | 0/0 | 2229 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0009 | 0/0 | 2229 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0010 | 0/0 | 2229 | 4 | 0 | 4 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0011 | 0/0 | 2229 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0012 | 0/0 | 2229 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0013 | 0/0 | 2229 | 2 | 0 | 1 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0014 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0015 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0016 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0017 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0018 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0019 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| c0020 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| 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 | 3203 | 107 | 4 | 19 | 63 | 3 | 17 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0002 | 0/0 | 3204 | 69 | 12 | 17 | 36 | 1 | 3 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0003 | 1/0 | 3203 | 35 | 1 | 14 | 11 | 5 | 3 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0004 | 0/0 | 3204 | 33 | 0 | 8 | 20 | 0 | 5 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0005 | 0/0 | 3203 | 25 | 10 | 0 | 14 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0006 | 0/0 | 3203 | 23 | 17 | 0 | 6 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0007 | 0/0 | 3204 | 14 | 11 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0008 | 0/0 | 3204 | 10 | 5 | 1 | 4 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0009 | 0/0 | 3204 | 7 | 7 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0010 | 0/0 | 3204 | 6 | 1 | 3 | 0 | 1 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0011 | 0/0 | 3204 | 5 | 2 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0012 | 0/0 | 3203 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0013 | 0/0 | 3204 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0014 | 0/0 | 3204 | 3 | 1 | 1 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0015 | 0/0 | 18875 | 3 | 0 | 0 | 3 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0016 | 0/0 | 3203 | 3 | 0 | 0 | 3 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0017 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0018 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0019 | 0/0 | 3203 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0020 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0021 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0022 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0023 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0024 | 0/0 | 3203 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0025 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0026 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0027 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0028 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0029 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0030 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0031 | 0/0 | 3203 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0032 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0033 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0034 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0035 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0036 | 0/0 | 3203 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0037 | 0/0 | 3203 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0038 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| t0039 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| 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 | 0 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2229 | 254 | 38 | 32 | 149 | 7 | 27 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002 | 0/0 | 2229 | 25 | 24 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004 | 0/0 | 2229 | 21 | 5 | 6 | 8 | 0 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007 | 0/0 | 2229 | 8 | 7 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0008 | 0/0 | 2229 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0010 | 0/0 | 2229 | 4 | 0 | 4 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0011 | 0/0 | 2229 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0014 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0017 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0019 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003 | 0/0 | 2229 | 22 | 6 | 9 | 4 | 1 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005 | 0/0 | 2229 | 15 | 1 | 8 | 5 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0003c0006 | 1/0 | 2229 | 8 | 0 | 6 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0003c0018 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0004c0009 | 0/0 | 2229 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0005c0012 | 0/0 | 2229 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0005c0013 | 0/0 | 2229 | 2 | 0 | 1 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0006c0015 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0007c0016 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0008c0020 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5431 | 88 | 1 | 14 | 55 | 3 | 14 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0002 | 0/0 | 5432 | 41 | 2 | 5 | 30 | 1 | 3 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0003 | 0/0 | 5431 | 18 | 0 | 3 | 10 | 3 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0004 | 0/0 | 5432 | 26 | 0 | 5 | 18 | 0 | 3 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0005 | 0/0 | 5431 | 17 | 3 | 0 | 13 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0006 | 0/0 | 5431 | 20 | 14 | 0 | 6 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0007 | 0/0 | 5432 | 6 | 6 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0008 | 0/0 | 5432 | 5 | 3 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0009 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0010 | 0/0 | 5432 | 3 | 0 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0012 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0013 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0014 | 0/0 | 5432 | 2 | 0 | 1 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0015 | 0/0 | 21103 | 3 | 0 | 0 | 3 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0016 | 0/0 | 5431 | 3 | 0 | 0 | 3 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0018 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0019 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0020 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0021 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0022 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0023 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0024 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0025 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0028 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0031 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0032 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0034 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0035 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0036 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0001t0037 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0001 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0002 | 0/0 | 5432 | 5 | 5 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0003 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0005 | 0/0 | 5431 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0006 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0007 | 0/0 | 5432 | 3 | 3 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0008 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0009 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0012 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0029 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0002t0038 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0001 | 0/0 | 5431 | 7 | 1 | 4 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0002 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0003 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0004 | 0/0 | 5432 | 4 | 0 | 2 | 0 | 0 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0007 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0008 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0013 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0004t0019 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007t0002 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007t0005 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007t0011 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0007t0026 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0008t0002 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0008t0005 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0008t0014 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0010t0007 | 0/0 | 5432 | 3 | 0 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0010t0033 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0011t0001 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0014t0003 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0017t0001 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0001c0019t0030 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0001 | 0/0 | 5431 | 4 | 0 | 1 | 1 | 0 | 2 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0002 | 0/0 | 5432 | 3 | 0 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0003 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0004 | 0/0 | 5432 | 2 | 0 | 1 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0005 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0007 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0009 | 0/0 | 5432 | 4 | 4 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0010 | 0/0 | 5432 | 2 | 1 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0011 | 0/0 | 5432 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0027 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0003t0039 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0001 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0002 | 0/0 | 5432 | 10 | 0 | 8 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0004 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0008 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0009 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0002c0005t0010 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0003c0006t0003 | 1/0 | 5431 | 8 | 0 | 6 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0003c0018t0003 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0004c0009t0002 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0004c0009t0017 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0005c0012t0003 | 0/0 | 5431 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0005c0013t0003 | 0/0 | 5431 | 2 | 0 | 1 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0006c0015t0001 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0007c0016t0011 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| a0008c0020t0001 | 0/0 | 5450 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | copy fasta | chr11 | 35134171 | 35237402 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0006g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0014g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0014g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0015g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0018g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0018g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0020g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0020g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0021g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0022g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0023g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0024g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0025g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0028g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0031g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0032g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0034g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0035g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0036g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0001t0037g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0007g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0008g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0029g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0002t0038g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0013g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0004t0019g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0011g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0007t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0008t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0008t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0008t0005g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0008t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0010t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0010t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0010t0007g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0010t0033g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0011t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0014t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0017t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0001c0019t0030g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0011g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0027g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0003t0039g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0002c0005t0010g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0006t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0003c0018t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0004c0009t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0004c0009t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0004c0009t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0004c0009t0017g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0005c0012t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0005c0013t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0005c0013t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0006c0015t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0007c0016t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| a0008c0020t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00099 | hp2 | a0002 | c0003 | t0010 | g0233 | EUR | GBR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0111 | EUR | GBR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | GBR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00323 | hp1 | a0005 | c0013 | t0003 | g0017 | EUR | FIN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00408 | hp1 | a0001 | c0001 | t0015 | g0044 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00408 | hp2 | a0001 | c0004 | t0008 | g0247 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00639 | hp1 | a0005 | c0012 | t0003 | g0011 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00639 | hp2 | a0001 | c0004 | t0004 | g0058 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00673 | hp1 | a0001 | c0001 | t0020 | g0344 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00673 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | CHS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00733 | hp1 | a0001 | c0001 | t0014 | g0259 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00733 | hp2 | a0002 | c0003 | t0027 | g0358 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00735 | hp1 | a0003 | c0018 | t0003 | g0060 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0257 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0112 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00738 | hp2 | a0003 | c0006 | t0003 | g0071 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00741 | hp1 | a0002 | c0003 | t0003 | g0067 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01070 | hp2 | a0002 | c0003 | t0011 | g0127 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01071 | hp1 | a0002 | c0003 | t0011 | g0128 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01074 | hp2 | a0005 | c0013 | t0003 | g0352 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01081 | hp1 | a0001 | c0010 | t0033 | g0187 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01099 | hp2 | a0007 | c0016 | t0011 | g0055 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01109 | hp2 | a0001 | c0001 | t0022 | g0090 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0072 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0073 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01192 | hp2 | a0003 | c0006 | t0003 | g0341 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01243 | hp1 | a0005 | c0012 | t0003 | g0011 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01243 | hp2 | a0001 | c0002 | t0008 | g0303 | AMR | PUR | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01255 | hp2 | a0002 | c0005 | t0002 | g0001 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01256 | hp1 | a0001 | c0010 | t0007 | g0162 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01257 | hp2 | a0002 | c0005 | t0002 | g0263 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01258 | hp1 | a0002 | c0005 | t0002 | g0264 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01258 | hp2 | a0001 | c0010 | t0007 | g0161 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0353 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01346 | hp1 | a0002 | c0005 | t0002 | g0001 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01358 | hp2 | a0003 | c0006 | t0003 | g0340 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0232 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01433 | hp2 | a0003 | c0006 | t0003 | g0342 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01496 | hp1 | a0001 | c0007 | t0002 | g0301 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0080 | EUR | IBS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01515 | hp2 | a0003 | c0006 | t0003 | g0329 | EUR | IBS | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0302 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0360 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01891 | hp1 | a0004 | c0009 | t0002 | g0300 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01891 | hp2 | a0002 | c0003 | t0009 | g0181 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01928 | hp2 | a0002 | c0005 | t0002 | g0262 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01943 | hp2 | a0002 | c0005 | t0002 | g0282 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01952 | hp1 | a0002 | c0005 | t0002 | g0001 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01952 | hp2 | a0002 | c0003 | t0004 | g0057 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01975 | hp1 | a0002 | c0003 | t0002 | g0056 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0276 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0277 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01981 | hp2 | a0003 | c0006 | t0003 | g0123 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0265 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02027 | hp2 | a0001 | c0001 | t0020 | g0365 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02040 | hp1 | a0001 | c0017 | t0001 | g0283 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02055 | hp1 | a0002 | c0003 | t0010 | g0015 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02071 | hp2 | a0002 | c0003 | t0005 | g0152 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02080 | hp1 | a0001 | c0001 | t0035 | g0156 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02080 | hp2 | a0001 | c0001 | t0015 | g0051 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02083 | hp1 | a0001 | c0001 | t0015 | g0043 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02132 | hp1 | a0002 | c0005 | t0008 | g0248 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0339 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | KHV | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0231 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02148 | hp2 | a0002 | c0003 | t0002 | g0255 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CDX | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0096 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02257 | hp2 | a0001 | c0002 | t0009 | g0182 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02258 | hp2 | a0001 | c0004 | t0007 | g0364 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02273 | hp2 | a0002 | c0005 | t0002 | g0274 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0165 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0104 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02300 | hp1 | a0001 | c0004 | t0004 | g0119 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02300 | hp2 | a0001 | c0010 | t0007 | g0133 | AMR | PEL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02451 | hp1 | a0001 | c0007 | t0002 | g0296 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02572 | hp1 | a0001 | c0002 | t0007 | g0012 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0297 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02615 | hp2 | a0002 | c0003 | t0009 | g0179 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02630 | hp2 | a0004 | c0009 | t0017 | g0092 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02683 | hp1 | a0006 | c0015 | t0001 | g0077 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02698 | hp2 | a0001 | c0014 | t0003 | g0064 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0299 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0178 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0354 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02886 | hp2 | a0001 | c0007 | t0011 | g0087 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0359 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02895 | hp2 | a0001 | c0004 | t0013 | g0003 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02897 | hp2 | a0001 | c0004 | t0013 | g0003 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02970 | hp1 | a0001 | c0007 | t0005 | g0185 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0102 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02976 | hp2 | a0004 | c0009 | t0017 | g0241 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03017 | hp2 | a0001 | c0001 | t0037 | g0316 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0106 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03041 | hp2 | a0001 | c0001 | t0021 | g0091 | AFR | GWD | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03098 | hp1 | a0001 | c0008 | t0005 | g0362 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03130 | hp1 | a0002 | c0003 | t0007 | g0188 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0171 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03195 | hp1 | a0001 | c0007 | t0011 | g0088 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0304 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03209 | hp2 | a0001 | c0008 | t0014 | g0172 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03225 | hp1 | a0001 | c0008 | t0002 | g0347 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03225 | hp2 | a0002 | c0005 | t0009 | g0167 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03453 | hp1 | a0001 | c0007 | t0026 | g0100 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03453 | hp2 | a0001 | c0008 | t0005 | g0363 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03486 | hp1 | a0001 | c0004 | t0019 | g0054 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0093 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0244 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0245 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03516 | hp2 | a0001 | c0001 | t0028 | g0251 | AFR | ESN | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0095 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0194 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03704 | hp2 | a0001 | c0001 | t0031 | g0126 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03710 | hp2 | a0001 | c0004 | t0004 | g0059 | SAS | PJL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03834 | hp1 | a0001 | c0001 | t0036 | g0326 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03927 | hp2 | a0001 | c0001 | t0024 | g0053 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG04199 | hp1 | a0001 | c0004 | t0004 | g0018 | SAS | STU | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG04228 | hp1 | a0002 | c0005 | t0010 | g0284 | SAS | STU | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18522 | hp1 | a0001 | c0002 | t0029 | g0183 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0097 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18612 | hp1 | a0002 | c0003 | t0039 | g0216 | EAS | CHB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18906 | hp1 | a0002 | c0003 | t0009 | g0180 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18939 | hp1 | a0002 | c0005 | t0002 | g0281 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18943 | hp1 | a0002 | c0005 | t0002 | g0267 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18952 | hp1 | a0001 | c0001 | t0018 | g0046 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18957 | hp1 | a0001 | c0001 | t0032 | g0279 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0333 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18961 | hp2 | a0001 | c0004 | t0002 | g0273 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18965 | hp1 | a0001 | c0001 | t0016 | g0078 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18966 | hp2 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18967 | hp1 | a0008 | c0020 | t0001 | g0237 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18972 | hp2 | a0001 | c0004 | t0002 | g0275 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18975 | hp2 | a0002 | c0005 | t0004 | g0268 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18983 | hp2 | a0001 | c0011 | t0001 | g0008 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0355 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18987 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18989 | hp1 | a0001 | c0004 | t0002 | g0272 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18989 | hp2 | a0002 | c0003 | t0004 | g0039 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0328 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19005 | hp1 | a0001 | c0001 | t0014 | g0025 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0361 | AFR | LWK | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19030 | hp2 | a0001 | c0002 | t0038 | g0103 | AFR | LWK | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19043 | hp1 | a0001 | c0019 | t0030 | g0350 | AFR | LWK | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19043 | hp2 | a0001 | c0007 | t0006 | g0098 | AFR | LWK | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19063 | hp1 | a0001 | c0004 | t0001 | g0271 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19065 | hp2 | a0001 | c0001 | t0016 | g0155 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19066 | hp2 | a0001 | c0001 | t0034 | g0120 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19067 | hp1 | a0001 | c0001 | t0018 | g0045 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19070 | hp1 | a0002 | c0005 | t0001 | g0269 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19087 | hp2 | a0001 | c0001 | t0023 | g0021 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19088 | hp1 | a0001 | c0011 | t0001 | g0008 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19088 | hp2 | a0001 | c0004 | t0002 | g0270 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0199 | AFR | ASW | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20129 | hp2 | a0001 | c0007 | t0002 | g0099 | AFR | ASW | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | GIH | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01123 | hp1 | a0003 | c0006 | t0003 | g0346 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | CLM | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0101 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0295 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG02559 | hp2 | a0004 | c0009 | t0002 | g0186 | AFR | ACB | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG03471 | hp2 | a0001 | c0001 | t0025 | g0066 | AFR | MSL | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | USA | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| HG06807 | hp2 | a0001 | c0002 | t0007 | g0305 | AFR | USA | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20300 | hp1 | a0002 | c0003 | t0009 | g0218 | AFR | USA | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | USA | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| homoSapiens_grch38 | hp1 | a0003 | c0006 | t0003 | g0324 | REF | REF | CD44_chr11_35134171_35237402 | CD44 | chr11 | 35134171 | 35237402 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:35176590
|
G | GCCGCTTT others(12): Show |
1 | a0008 | 1 | NA18967.hp1 | frameshift_variant | HIGH | c.85_103dupCGCTTTGCA others(10): Show |
p.His35fs | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/18 | 237/5431 | 104/2229 | 35/742 | INFO_REALIGN_3_PRIME | chr11 | 35176590 | |
| chr11:35176644
|
G | C | 1 | a0006 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.137G>C | p.Arg46Pro | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/18 | 270/5431 | 137/2229 | 46/742 | chr11 | 35176644 | ||
| chr11:35204608
|
A | G | 6 | a0001a0004a0005others(3): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
missense_variant | MODERATE | c.1250A>G | p.Lys417Arg | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/18 | 1383/5431 | 1250/2229 | 417/742 | chr11 | 35204608 | ||
| chr11:35206211
|
T | C | 1 | a0007 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1382T>C | p.Met461Thr | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/18 | 1515/5431 | 1382/2229 | 461/742 | chr11 | 35206211 | ||
| chr11:35206217
|
G | A | 1 | a0004 | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.1388G>A | p.Arg463Gln | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/18 | 1521/5431 | 1388/2229 | 463/742 | chr11 | 35206217 | ||
| chr11:35208126
|
T | C | 6 | a0001a0002a0004others(3): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
missense_variant | MODERATE | c.1436T>C | p.Ile479Thr | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/18 | 1569/5431 | 1436/2229 | 479/742 | chr11 | 35208126 | ||
| chr11:35219328
|
G | T | 1 | a0006 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1886G>T | p.Gly629Val | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/18 | 2019/5431 | 1886/2229 | 629/742 | chr11 | 35219328 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:35139348
|
G | C | 1 | a0001c0014 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.45G>C | p.Val15Val | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/18 | 178/5431 | 45/2229 | 15/742 | chr11 | 35139348 | ||
| chr11:35180295
|
C | T | 6 | a0001c0004a0001c0007a0001c0019others(3): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
synonymous_variant | LOW | c.255C>T | p.His85His | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/18 | 388/5431 | 255/2229 | 85/742 | chr11 | 35180295 | ||
| chr11:35189887
|
G | A | 1 | a0001c0008 | 4 | HG03098.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.489G>A | p.Thr163Thr | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/18 | 622/5431 | 489/2229 | 163/742 | chr11 | 35189887 | ||
| chr11:35196813
|
T | C | 1 | a0001c0008 | 4 | HG03098.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.735T>C | p.Phe245Phe | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/18 | 868/5431 | 735/2229 | 245/742 | chr11 | 35196813 | ||
| chr11:35201134
|
C | T | 1 | a0001c0010 | 4 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
synonymous_variant | LOW | c.975C>T | p.Thr325Thr | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 8/18 | 1108/5431 | 975/2229 | 325/742 | chr11 | 35201134 | ||
| chr11:35201756
|
G | A | 3 | a0001c0002a0001c0007a0007c0016 | 34 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(31): Show |
synonymous_variant | LOW | c.1122G>A | p.Glu374Glu | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/18 | 1255/5431 | 1122/2229 | 374/742 | chr11 | 35201756 | ||
| chr11:35206215
|
A | G | 1 | a0001c0019 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1386A>G | p.Gly462Gly | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/18 | 1519/5431 | 1386/2229 | 462/742 | chr11 | 35206215 | ||
| chr11:35211340
|
G | A | 1 | a0001c0011 | 2 | NA18983.hp2 NA19088.hp1 |
synonymous_variant | LOW | c.1701G>A | p.Thr567Thr | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/18 | 1834/5431 | 1701/2229 | 567/742 | chr11 | 35211340 | ||
| chr11:35221703
|
A | G | 1 | a0001c0017 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.1995A>G | p.Ala665Ala | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/18 | 2128/5431 | 1995/2229 | 665/742 | chr11 | 35221703 | ||
| chr11:35229168
|
T | C | 1 | a0006c0015 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.2064T>C | p.Asn688Asn | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2197/5431 | 2064/2229 | 688/742 | chr11 | 35229168 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:35139292
|
G | A | 3 | a0001c0001t0021a0001c0001t0022a0004c0009t0017 | 4 | HG01109.hp2 HG02630.hp2 HG02976.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/18 | 12 | chr11 | 35139292 | |||||
| chr11:35229334
|
C | G | 1 | a0002c0003t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1 | chr11 | 35229334 | |||||
| chr11:35229471
|
T | C | 4 | a0001c0001t0008a0001c0002t0008a0001c0004t0008others(1): Show | 10 | HG00408.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*138T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 138 | chr11 | 35229471 | |||||
| chr11:35229682
|
A | G | 3 | a0001c0001t0013a0001c0002t0038a0001c0004t0013 | 5 | HG02895.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*349A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 349 | chr11 | 35229682 | |||||
| chr11:35229771
|
C | T | 20 | a0001c0001t0001a0001c0001t0012a0001c0001t0016others(17): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 438 | chr11 | 35229771 | |||||
| chr11:35229922
|
C | T | 1 | a0001c0001t0037 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 589 | chr11 | 35229922 | |||||
| chr11:35230110
|
G | C | 1 | a0001c0001t0031 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*777G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 777 | chr11 | 35230110 | |||||
| chr11:35230215
|
G | T | 1 | a0001c0019t0030 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*882G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 882 | chr11 | 35230215 | |||||
| chr11:35230222
|
G | GT | 38 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(35): Show | 149 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*901dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 902 | INFO_REALIGN_3_PRIME | chr11 | 35230222 | ||||
| chr11:35230222
|
G | GTTTTTTT others(15665): Show |
1 | a0001c0001t0015 | 3 | HG00408.hp1 HG02080.hp2 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*901_*902insTGACAC others(15666): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 902 | INFO_REALIGN_3_PRIME | chr11 | 35230222 | ||||
| chr11:35230228
|
T | TG | 4 | a0001c0001t0008a0001c0002t0008a0001c0004t0008others(1): Show | 10 | HG00408.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*895_*896insG | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 896 | chr11 | 35230228 | |||||
| chr11:35230298
|
C | A | 3 | a0001c0001t0010a0002c0003t0010a0002c0005t0010 | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*965C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 965 | chr11 | 35230298 | |||||
| chr11:35230616
|
G | T | 1 | a0001c0019t0030 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1283G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1283 | chr11 | 35230616 | |||||
| chr11:35230808
|
T | C | 1 | a0001c0001t0032 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1475T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1475 | chr11 | 35230808 | |||||
| chr11:35230892
|
A | T | 4 | a0001c0001t0009a0001c0002t0009a0002c0003t0009others(1): Show | 7 | HG01891.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1559A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1559 | chr11 | 35230892 | |||||
| chr11:35230907
|
C | T | 1 | a0001c0001t0036 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1574C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1574 | chr11 | 35230907 | |||||
| chr11:35230915
|
G | C | 1 | a0002c0003t0027 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1582G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1582 | chr11 | 35230915 | |||||
| chr11:35230997
|
G | A | 7 | a0001c0001t0005a0001c0001t0018a0001c0001t0023others(4): Show | 28 | HG02071.hp1 HG02071.hp2 HG02109.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1664 | chr11 | 35230997 | |||||
| chr11:35231052
|
T | C | 1 | a0001c0001t0028 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1719T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1719 | chr11 | 35231052 | |||||
| chr11:35231076
|
C | T | 1 | a0001c0001t0018 | 2 | NA18952.hp1 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1743C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1743 | chr11 | 35231076 | |||||
| chr11:35231158
|
G | A | 1 | a0001c0001t0016 | 3 | NA18956.hp1 NA18965.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1825G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1825 | chr11 | 35231158 | |||||
| chr11:35231186
|
T | C | 1 | a0001c0001t0023 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1853T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1853 | chr11 | 35231186 | |||||
| chr11:35231193
|
G | C | 1 | a0001c0002t0029 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 1860 | chr11 | 35231193 | |||||
| chr11:35231379
|
C | T | 13 | a0001c0001t0007a0001c0001t0013a0001c0001t0019others(10): Show | 24 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2046C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2046 | chr11 | 35231379 | |||||
| chr11:35231450
|
C | G | 1 | a0001c0001t0020 | 2 | HG00673.hp1 HG02027.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2117C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2117 | chr11 | 35231450 | |||||
| chr11:35231586
|
C | T | 6 | a0001c0001t0004a0001c0001t0025a0001c0001t0035others(3): Show | 35 | HG00597.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2253C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2253 | chr11 | 35231586 | |||||
| chr11:35231669
|
G | A | 1 | a0001c0010t0033 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2336G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2336 | chr11 | 35231669 | |||||
| chr11:35231725
|
C | T | 45 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(42): Show | 156 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*2392C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2392 | chr11 | 35231725 | |||||
| chr11:35231731
|
T | G | 5 | a0001c0001t0021a0001c0007t0011a0001c0007t0026others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2398T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2398 | chr11 | 35231731 | |||||
| chr11:35231855
|
A | G | 1 | a0001c0001t0034 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2522 | chr11 | 35231855 | |||||
| chr11:35231896
|
T | C | 2 | a0001c0001t0012a0001c0002t0012 | 4 | HG02280.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2563T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2563 | chr11 | 35231896 | |||||
| chr11:35232134
|
A | G | 1 | a0001c0001t0024 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2801A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 18/18 | 2801 | chr11 | 35232134 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:35139496
|
T | C | 2 | a0001c0001t0013g0013a0001c0002t0007g0012 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+126T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139496 | ||||||
| chr11:35139529
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(36): Show | 40 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+159T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139529 | ||||||
| chr11:35139613
|
C | T | 1 | a0001c0001t0001g0366 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.67+243C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139613 | ||||||
| chr11:35139738
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(36): Show | 40 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+368A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139738 | ||||||
| chr11:35139741
|
G | A | 32 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(29): Show | 32 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.67+371G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139741 | ||||||
| chr11:35139858
|
G | C | 1 | a0001c0001t0004g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.67+488G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139858 | ||||||
| chr11:35139859
|
G | T | 1 | a0001c0001t0004g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.67+489G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139859 | ||||||
| chr11:35139876
|
A | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(29): Show | 32 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.67+506A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35139876 | ||||||
| chr11:35140116
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.67+746G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140116 | ||||||
| chr11:35140123
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.67+753T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140123 | ||||||
| chr11:35140190
|
C | G | 1 | a0002c0005t0010g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67+820C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140190 | ||||||
| chr11:35140360
|
C | T | 1 | a0001c0001t0015g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.67+990C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140360 | ||||||
| chr11:35140488
|
C | T | 41 | a0001c0001t0001g0254a0001c0001t0001g0278a0001c0001t0002g0250others(38): Show | 43 | HG00408.hp2 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.67+1118C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140488 | ||||||
| chr11:35140619
|
C | A | 1 | a0001c0001t0005g0246 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+1249C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140619 | ||||||
| chr11:35140831
|
G | A | 3 | a0001c0004t0001g0249a0001c0004t0008g0247a0002c0005t0008g0248 | 3 | HG00408.hp2 HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.67+1461G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140831 | ||||||
| chr11:35140882
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+1512G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140882 | ||||||
| chr11:35140929
|
GAGAATTG others(98): Show |
G | 2 | a0002c0003t0001g0244a0002c0003t0001g0245 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.67+1561_67+1665del | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35140929 | |||||
| chr11:35140956
|
G | T | 1 | a0001c0001t0004g0050 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.67+1586G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35140956 | ||||||
| chr11:35141018
|
TA | T | 40 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0278others(37): Show | 43 | HG00408.hp2 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.67+1661delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35141018 | |||||
| chr11:35141050
|
C | T | 1 | a0001c0001t0020g0365 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.67+1680C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141050 | ||||||
| chr11:35141061
|
A | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | NA18940.hp2 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1691A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141061 | ||||||
| chr11:35141254
|
T | C | 45 | a0001c0001t0001g0089a0001c0001t0001g0254a0001c0001t0001g0278others(42): Show | 47 | HG00408.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+1884T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141254 | ||||||
| chr11:35141315
|
AT | A | 11 | a0001c0001t0001g0009a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 12 | HG00544.hp2 HG01071.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+1948delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35141315 | |||||
| chr11:35141567
|
T | C | 32 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(29): Show | 32 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.67+2197T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141567 | ||||||
| chr11:35141663
|
C | T | 1 | a0001c0004t0007g0364 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+2293C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141663 | ||||||
| chr11:35141666
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0002g0235 | 2 | HG01192.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.67+2296A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141666 | ||||||
| chr11:35141668
|
T | G | 45 | a0001c0001t0001g0089a0001c0001t0001g0254a0001c0001t0001g0278others(42): Show | 47 | HG00408.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+2298T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141668 | ||||||
| chr11:35141701
|
T | C | 1 | a0001c0002t0002g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+2331T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141701 | ||||||
| chr11:35141726
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0010g0232a0002c0003t0010g0233 | 3 | HG00099.hp2 HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.67+2356C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141726 | ||||||
| chr11:35141756
|
G | A | 1 | a0002c0003t0010g0015 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+2386G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141756 | ||||||
| chr11:35141855
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(240): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.67+2485G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141855 | ||||||
| chr11:35141915
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(240): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.67+2545G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141915 | ||||||
| chr11:35141939
|
C | T | 289 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(286): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.67+2569C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35141939 | ||||||
| chr11:35142092
|
C | T | 5 | a0001c0001t0001g0089a0001c0002t0005g0231a0001c0007t0011g0087others(2): Show | 5 | HG02145.hp1 HG02738.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2722C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142092 | ||||||
| chr11:35142179
|
T | C | 4 | a0001c0001t0021g0091a0001c0001t0022g0090a0004c0009t0017g0092others(1): Show | 4 | HG01109.hp2 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2809T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142179 | ||||||
| chr11:35142196
|
T | C | 14 | a0001c0001t0001g0089a0001c0001t0007g0094a0001c0001t0007g0095others(11): Show | 15 | HG02145.hp1 HG02257.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+2826T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142196 | ||||||
| chr11:35142370
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67+3000T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142370 | ||||||
| chr11:35142413
|
C | T | 12 | a0001c0001t0001g0230a0001c0001t0001g0243a0001c0001t0002g0220others(9): Show | 12 | HG00544.hp1 HG02027.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+3043C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142413 | ||||||
| chr11:35142427
|
G | A | 7 | a0001c0001t0005g0307a0001c0001t0006g0304a0001c0002t0001g0306others(4): Show | 7 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+3057G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142427 | ||||||
| chr11:35142457
|
C | A | 1 | a0001c0002t0005g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+3087C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142457 | ||||||
| chr11:35142461
|
G | A | 1 | a0001c0002t0005g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+3091G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142461 | ||||||
| chr11:35142561
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(290): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.67+3191C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142561 | ||||||
| chr11:35142580
|
T | C | 3 | a0001c0001t0008g0295a0001c0002t0002g0297a0001c0007t0002g0296 | 3 | HG02109.hp2 HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+3210T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142580 | ||||||
| chr11:35142620
|
T | A | 1 | a0001c0002t0005g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67+3250T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142620 | ||||||
| chr11:35142705
|
C | A | 2 | a0001c0002t0008g0102a0001c0002t0038g0103 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+3335C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142705 | ||||||
| chr11:35142875
|
A | T | 1 | a0002c0003t0027g0358 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.67+3505A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142875 | ||||||
| chr11:35142971
|
C | G | 2 | a0001c0002t0001g0219a0002c0003t0009g0218 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.67+3601C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142971 | ||||||
| chr11:35142999
|
G | A | 4 | a0001c0001t0007g0107a0001c0001t0009g0105a0001c0002t0006g0104others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+3629G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35142999 | ||||||
| chr11:35143080
|
C | T | 1 | a0001c0001t0003g0357 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+3710C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143080 | ||||||
| chr11:35143188
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67+3818T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143188 | ||||||
| chr11:35143329
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.67+3959C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143329 | ||||||
| chr11:35143484
|
G | A | 3 | a0001c0001t0002g0250a0001c0001t0008g0252a0001c0001t0028g0251 | 3 | HG02723.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+4114G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143484 | ||||||
| chr11:35143532
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67+4162C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143532 | ||||||
| chr11:35143533
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.67+4163G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143533 | ||||||
| chr11:35143538
|
A | G | 2 | a0001c0001t0005g0355a0001c0001t0005g0356 | 2 | NA18968.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.67+4168A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143538 | ||||||
| chr11:35143588
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.67+4218T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143588 | ||||||
| chr11:35143591
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(201): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.67+4221C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143591 | ||||||
| chr11:35143606
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67+4236T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143606 | ||||||
| chr11:35143726
|
C | CTGGCCTG others(14): Show |
42 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(39): Show | 45 | HG00438.hp1 HG00621.hp2 HG02015.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+4362_67+4382dup others(21): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35143726 | |||||
| chr11:35143963
|
G | A | 8 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4593G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35143963 | ||||||
| chr11:35144055
|
C | G | 13 | a0001c0001t0001g0089a0001c0001t0001g0190a0001c0001t0001g0234others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+4685C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144055 | ||||||
| chr11:35144160
|
G | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(11): Show | 14 | NA18946.hp1 NA18948.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+4790G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144160 | ||||||
| chr11:35144253
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(206): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.67+4883G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144253 | ||||||
| chr11:35144263
|
C | A | 3 | a0001c0001t0006g0168a0001c0001t0012g0005a0001c0004t0007g0364 | 4 | HG02258.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4893C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144263 | ||||||
| chr11:35144289
|
G | A | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+4919G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144289 | ||||||
| chr11:35144308
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0086 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.67+4938C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144308 | ||||||
| chr11:35144419
|
G | A | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+5049G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144419 | ||||||
| chr11:35144421
|
T | A | 6 | a0001c0001t0006g0006a0001c0001t0006g0191a0001c0001t0006g0192others(3): Show | 7 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+5051T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144421 | ||||||
| chr11:35144575
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.67+5205C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144575 | ||||||
| chr11:35144684
|
G | A | 1 | a0002c0005t0002g0262 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67+5314G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144684 | ||||||
| chr11:35144816
|
C | G | 2 | a0001c0001t0005g0355a0001c0001t0005g0356 | 2 | NA18968.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.67+5446C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144816 | ||||||
| chr11:35144859
|
C | A | 1 | a0001c0001t0024g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.67+5489C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144859 | ||||||
| chr11:35144955
|
C | A | 6 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+5585C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35144955 | ||||||
| chr11:35145099
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0002g0032 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.67+5729T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145099 | ||||||
| chr11:35145101
|
C | T | 1 | a0001c0002t0005g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67+5731C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145101 | ||||||
| chr11:35145188
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.67+5818C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145188 | ||||||
| chr11:35145251
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(98): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.67+5881C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145251 | ||||||
| chr11:35145324
|
T | C | 2 | a0001c0002t0002g0253a0001c0008t0014g0172 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67+5954T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145324 | ||||||
| chr11:35145513
|
C | T | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+6143C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145513 | ||||||
| chr11:35145521
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0310 | 3 | NA19007.hp2 NA19012.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.67+6151G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145521 | ||||||
| chr11:35145556
|
T | C | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+6186T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145556 | ||||||
| chr11:35145734
|
T | G | 5 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6364T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145734 | ||||||
| chr11:35145812
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.67+6442G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145812 | ||||||
| chr11:35145846
|
C | A | 5 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | NA18967.hp2 NA18991.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6476C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145846 | ||||||
| chr11:35145899
|
C | T | 7 | a0001c0001t0001g0163a0001c0001t0021g0091a0001c0002t0006g0104others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+6529C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145899 | ||||||
| chr11:35145900
|
G | A | 8 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+6530G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145900 | ||||||
| chr11:35145928
|
C | T | 4 | a0001c0001t0005g0170a0001c0002t0008g0102a0001c0002t0008g0171others(1): Show | 4 | HG02647.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6558C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145928 | ||||||
| chr11:35145994
|
C | T | 25 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(22): Show | 27 | HG00438.hp1 HG00621.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.67+6624C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35145994 | ||||||
| chr11:35146056
|
G | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.67+6686G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146056 | ||||||
| chr11:35146116
|
T | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0110a0001c0001t0003g0111others(1): Show | 4 | HG00140.hp1 HG00738.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6746T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146116 | ||||||
| chr11:35146480
|
T | C | 10 | a0001c0001t0002g0261a0001c0001t0005g0170a0001c0001t0006g0166others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+7110T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146480 | ||||||
| chr11:35146504
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.67+7134C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146504 | ||||||
| chr11:35146516
|
G | A | 11 | a0001c0001t0001g0089a0001c0004t0004g0018a0001c0004t0013g0003others(8): Show | 12 | HG00323.hp1 HG01496.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+7146G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146516 | ||||||
| chr11:35146535
|
A | G | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.67+7165A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146535 | ||||||
| chr11:35146740
|
G | T | 1 | a0001c0001t0006g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.67+7370G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146740 | ||||||
| chr11:35146828
|
C | A | 3 | a0001c0001t0006g0168a0001c0001t0012g0005a0001c0004t0007g0364 | 4 | HG02258.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+7458C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146828 | ||||||
| chr11:35146971
|
A | G | 2 | a0001c0010t0007g0161a0001c0010t0007g0162 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.67+7601A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146971 | ||||||
| chr11:35146983
|
A | G | 1 | a0004c0009t0017g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.67+7613A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146983 | ||||||
| chr11:35146999
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(298): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.67+7629C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35146999 | ||||||
| chr11:35147034
|
GAGGGATG others(41): Show |
G | 1 | a0002c0005t0002g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.67+7695_67+7742del others(48): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35147034 | |||||
| chr11:35147075
|
G | A | 10 | a0001c0001t0002g0261a0001c0001t0005g0170a0001c0001t0006g0166others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+7705G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147075 | ||||||
| chr11:35147142
|
G | T | 20 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(17): Show | 20 | HG00408.hp1 HG02080.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+7772G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147142 | ||||||
| chr11:35147145
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(68): Show | 73 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.67+7775A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147145 | ||||||
| chr11:35147187
|
C | T | 1 | a0001c0001t0002g0348 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.67+7817C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147187 | ||||||
| chr11:35147279
|
A | T | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+7909A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147279 | ||||||
| chr11:35147371
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(70): Show | 75 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.67+8001A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147371 | ||||||
| chr11:35147448
|
A | G | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+8078A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147448 | ||||||
| chr11:35147484
|
A | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.67+8114A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147484 | ||||||
| chr11:35147515
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.67+8145G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147515 | ||||||
| chr11:35147526
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.67+8156C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147526 | ||||||
| chr11:35147574
|
G | T | 1 | a0002c0005t0002g0281 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.67+8204G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147574 | ||||||
| chr11:35147600
|
A | T | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+8230A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147600 | ||||||
| chr11:35147603
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.67+8233C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147603 | ||||||
| chr11:35147616
|
C | CT | 105 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(102): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.67+8258dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35147616 | |||||
| chr11:35147797
|
C | G | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 14 | HG00621.hp2 HG02015.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+8427C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147797 | ||||||
| chr11:35147948
|
G | A | 3 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0012g0165 | 3 | HG02109.hp2 HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67+8578G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35147948 | ||||||
| chr11:35148079
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67+8709G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148079 | ||||||
| chr11:35148091
|
C | CA | 7 | a0001c0001t0001g0208a0001c0001t0001g0289a0001c0001t0002g0206others(4): Show | 7 | HG00408.hp2 HG00673.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+8733dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35148091 | |||||
| chr11:35148104
|
G | A | 9 | a0001c0001t0005g0307a0001c0001t0006g0304a0001c0002t0001g0306others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+8734G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148104 | ||||||
| chr11:35148107
|
G | T | 9 | a0001c0001t0005g0307a0001c0001t0006g0304a0001c0002t0001g0306others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+8737G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148107 | ||||||
| chr11:35148141
|
A | G | 2 | a0001c0007t0002g0296a0002c0005t0009g0167 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.67+8771A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148141 | ||||||
| chr11:35148308
|
G | A | 100 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.67+8938G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148308 | ||||||
| chr11:35148329
|
G | C | 1 | a0001c0004t0019g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.67+8959G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148329 | ||||||
| chr11:35148763
|
A | G | 1 | a0001c0001t0007g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+9393A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148763 | ||||||
| chr11:35148997
|
T | C | 36 | a0001c0001t0001g0278a0001c0001t0002g0261a0001c0001t0002g0266others(33): Show | 38 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.67+9627T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35148997 | ||||||
| chr11:35149057
|
G | T | 1 | a0001c0001t0002g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.67+9687G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149057 | ||||||
| chr11:35149068
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+9698C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149068 | ||||||
| chr11:35149273
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+9903C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149273 | ||||||
| chr11:35149381
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(117): Show | 125 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.67+10011G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149381 | ||||||
| chr11:35149445
|
T | G | 1 | a0001c0001t0004g0118 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.67+10075T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149445 | ||||||
| chr11:35149480
|
G | A | 9 | a0001c0001t0005g0307a0001c0001t0006g0304a0001c0002t0001g0306others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+10110G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149480 | ||||||
| chr11:35149633
|
C | T | 2 | a0001c0007t0002g0296a0002c0005t0009g0167 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.67+10263C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149633 | ||||||
| chr11:35149905
|
C | G | 4 | a0001c0001t0005g0170a0001c0001t0007g0169a0001c0002t0008g0102others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+10535C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149905 | ||||||
| chr11:35149906
|
C | A | 4 | a0001c0001t0005g0170a0001c0001t0007g0169a0001c0002t0008g0102others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+10536C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149906 | ||||||
| chr11:35149918
|
T | C | 36 | a0001c0001t0001g0278a0001c0001t0002g0261a0001c0001t0002g0266others(33): Show | 38 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.67+10548T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149918 | ||||||
| chr11:35149965
|
G | A | 16 | a0001c0001t0001g0089a0001c0001t0021g0091a0001c0004t0004g0018others(13): Show | 17 | HG00323.hp1 HG01496.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+10595G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35149965 | ||||||
| chr11:35150070
|
T | TA | 221 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(218): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.67+10705dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35150070 | |||||
| chr11:35150136
|
T | G | 2 | a0001c0001t0002g0261a0001c0001t0007g0260 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67+10766T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150136 | ||||||
| chr11:35150194
|
T | C | 2 | a0002c0005t0002g0263a0002c0005t0002g0264 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.67+10824T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150194 | ||||||
| chr11:35150205
|
A | G | 1 | a0001c0001t0004g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+10835A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150205 | ||||||
| chr11:35150222
|
C | G | 2 | a0001c0008t0005g0362a0001c0008t0005g0363 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.67+10852C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150222 | ||||||
| chr11:35150398
|
C | T | 10 | a0001c0001t0002g0261a0001c0001t0005g0170a0001c0001t0006g0166others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+11028C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150398 | ||||||
| chr11:35150471
|
A | C | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0081 | 3 | HG01081.hp2 HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.67+11101A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150471 | ||||||
| chr11:35150507
|
T | A | 5 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(2): Show | 6 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+11137T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150507 | ||||||
| chr11:35150513
|
T | C | 1 | a0001c0004t0004g0119 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+11143T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150513 | ||||||
| chr11:35150562
|
C | T | 36 | a0001c0001t0001g0278a0001c0001t0002g0261a0001c0001t0002g0266others(33): Show | 38 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.67+11192C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150562 | ||||||
| chr11:35150575
|
G | A | 100 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.67+11205G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150575 | ||||||
| chr11:35150626
|
C | T | 1 | a0001c0001t0007g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+11256C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150626 | ||||||
| chr11:35150796
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.67+11426C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150796 | ||||||
| chr11:35150814
|
G | A | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+11444G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150814 | ||||||
| chr11:35150819
|
C | T | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+11449C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150819 | ||||||
| chr11:35150962
|
C | T | 1 | a0002c0003t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67+11592C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150962 | ||||||
| chr11:35150968
|
A | C | 3 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0012g0165 | 3 | HG02109.hp2 HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67+11598A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35150968 | ||||||
| chr11:35151061
|
T | C | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.67+11691T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151061 | ||||||
| chr11:35151110
|
T | C | 101 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.67+11740T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151110 | ||||||
| chr11:35151217
|
T | A | 139 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(136): Show | 144 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.67+11847T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151217 | ||||||
| chr11:35151481
|
C | T | 3 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0012g0165 | 3 | HG02109.hp2 HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67+12111C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151481 | ||||||
| chr11:35151596
|
G | A | 4 | a0001c0001t0005g0170a0001c0001t0007g0169a0001c0002t0008g0102others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12226G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151596 | ||||||
| chr11:35151666
|
C | A | 1 | a0001c0001t0004g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.67+12296C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151666 | ||||||
| chr11:35151798
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.67+12428A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151798 | ||||||
| chr11:35151930
|
G | A | 1 | a0007c0016t0011g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.67+12560G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151930 | ||||||
| chr11:35151977
|
A | T | 30 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(27): Show | 32 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.67+12607A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35151977 | ||||||
| chr11:35152020
|
C | T | 1 | a0001c0008t0002g0347 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67+12650C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152020 | ||||||
| chr11:35152174
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.67+12804A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152174 | ||||||
| chr11:35152177
|
T | C | 26 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(23): Show | 28 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+12807T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152177 | ||||||
| chr11:35152302
|
G | A | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0081 | 3 | HG01081.hp2 HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.67+12932G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152302 | ||||||
| chr11:35152427
|
A | C | 1 | a0003c0006t0003g0346 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+13057A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152427 | ||||||
| chr11:35152546
|
C | A | 1 | a0001c0001t0003g0312 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67+13176C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152546 | ||||||
| chr11:35152578
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+13208A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152578 | ||||||
| chr11:35152589
|
A | G | 139 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(136): Show | 144 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.67+13219A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152589 | ||||||
| chr11:35152741
|
G | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+13371G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152741 | ||||||
| chr11:35152778
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67+13408C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152778 | ||||||
| chr11:35152821
|
C | G | 1 | a0001c0002t0029g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+13451C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35152821 | ||||||
| chr11:35153048
|
G | A | 89 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(86): Show | 92 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.67+13678G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153048 | ||||||
| chr11:35153082
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.67+13712G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153082 | ||||||
| chr11:35153132
|
A | G | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+13762A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153132 | ||||||
| chr11:35153171
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(1): Show | 4 | HG00438.hp1 NA18952.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+13801C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153171 | ||||||
| chr11:35153219
|
A | G | 4 | a0001c0001t0005g0170a0001c0001t0007g0169a0001c0002t0008g0102others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+13849A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153219 | ||||||
| chr11:35153221
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67+13851T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153221 | ||||||
| chr11:35153257
|
A | C | 5 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+13887A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153257 | ||||||
| chr11:35153350
|
C | A | 2 | a0001c0001t0002g0261a0001c0001t0007g0260 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67+13980C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153350 | ||||||
| chr11:35153373
|
C | A | 4 | a0001c0001t0006g0168a0001c0001t0012g0005a0001c0002t0002g0253others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+14003C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153373 | ||||||
| chr11:35153395
|
C | A | 2 | a0001c0001t0013g0013a0001c0007t0005g0185 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+14025C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153395 | ||||||
| chr11:35153498
|
T | C | 101 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.67+14128T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153498 | ||||||
| chr11:35153569
|
C | T | 1 | a0001c0001t0013g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+14199C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153569 | ||||||
| chr11:35153625
|
G | A | 1 | a0001c0001t0034g0120 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.67+14255G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153625 | ||||||
| chr11:35153669
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67+14299G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153669 | ||||||
| chr11:35153708
|
G | A | 4 | a0001c0001t0005g0170a0001c0001t0007g0169a0001c0002t0008g0102others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+14338G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153708 | ||||||
| chr11:35153723
|
G | A | 78 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(75): Show | 81 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.67+14353G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153723 | ||||||
| chr11:35153843
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(47): Show | 51 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+14473A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35153843 | ||||||
| chr11:35154107
|
A | G | 2 | a0001c0007t0002g0296a0002c0005t0009g0167 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.67+14737A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154107 | ||||||
| chr11:35154198
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.67+14828C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154198 | ||||||
| chr11:35154250
|
G | T | 1 | a0001c0001t0007g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67+14880G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154250 | ||||||
| chr11:35154304
|
C | T | 5 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+14934C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154304 | ||||||
| chr11:35154395
|
C | T | 1 | a0001c0001t0005g0280 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.67+15025C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154395 | ||||||
| chr11:35154524
|
T | C | 78 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(75): Show | 81 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.67+15154T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154524 | ||||||
| chr11:35154612
|
T | C | 132 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0065others(129): Show | 137 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.67+15242T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154612 | ||||||
| chr11:35154704
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.67+15334T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154704 | ||||||
| chr11:35154751
|
C | G | 8 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0238others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+15381C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154751 | ||||||
| chr11:35154790
|
C | T | 2 | a0001c0007t0002g0296a0002c0005t0009g0167 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.67+15420C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35154790 | ||||||
| chr11:35154888
|
GA | G | 27 | a0001c0001t0001g0278a0001c0001t0002g0266a0001c0001t0004g0265others(24): Show | 29 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+15520delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35154888 | |||||
| chr11:35155029
|
A | C | 8 | a0001c0001t0006g0006a0001c0001t0006g0191a0001c0001t0006g0192others(5): Show | 9 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+15659A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155029 | ||||||
| chr11:35155549
|
T | C | 2 | a0001c0001t0002g0261a0001c0001t0007g0260 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67+16179T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155549 | ||||||
| chr11:35155605
|
A | G | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+16235A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155605 | ||||||
| chr11:35155740
|
A | T | 1 | a0001c0001t0001g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.67+16370A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155740 | ||||||
| chr11:35155842
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+16472A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155842 | ||||||
| chr11:35155915
|
C | A | 1 | a0001c0001t0003g0313 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.67+16545C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155915 | ||||||
| chr11:35155922
|
G | T | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.67+16552G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155922 | ||||||
| chr11:35155932
|
C | T | 152 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(149): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.67+16562C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35155932 | ||||||
| chr11:35156005
|
T | C | 51 | a0001c0001t0001g0089a0001c0001t0001g0278a0001c0001t0002g0266others(48): Show | 54 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.67+16635T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156005 | ||||||
| chr11:35156043
|
G | A | 3 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0012g0178 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.67+16673G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156043 | ||||||
| chr11:35156117
|
C | T | 6 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+16747C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156117 | ||||||
| chr11:35156224
|
C | A | 52 | a0001c0001t0001g0089a0001c0001t0002g0266a0001c0001t0005g0246others(49): Show | 55 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+16854C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156224 | ||||||
| chr11:35156300
|
A | G | 52 | a0001c0001t0001g0089a0001c0001t0004g0265a0001c0001t0005g0246others(49): Show | 55 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+16930A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156300 | ||||||
| chr11:35156435
|
C | T | 22 | a0001c0001t0005g0246a0001c0001t0005g0280a0001c0004t0001g0249others(19): Show | 24 | HG00408.hp2 HG00673.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.67+17065C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156435 | ||||||
| chr11:35156502
|
C | A | 1 | a0001c0001t0004g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.67+17132C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156502 | ||||||
| chr11:35156544
|
A | G | 20 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0209others(17): Show | 21 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+17174A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156544 | ||||||
| chr11:35156756
|
G | C | 1 | a0001c0001t0001g0308 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67+17386G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156756 | ||||||
| chr11:35156858
|
C | T | 1 | a0002c0003t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+17488C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156858 | ||||||
| chr11:35156900
|
G | A | 2 | a0002c0005t0002g0267a0002c0005t0002g0281 | 2 | NA18939.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.67+17530G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156900 | ||||||
| chr11:35156984
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(193): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.67+17614A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35156984 | ||||||
| chr11:35157036
|
T | C | 58 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(55): Show | 60 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+17666T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157036 | ||||||
| chr11:35157046
|
G | A | 48 | a0001c0001t0001g0089a0001c0001t0005g0246a0001c0001t0005g0280others(45): Show | 51 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+17676G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157046 | ||||||
| chr11:35157091
|
G | A | 45 | a0001c0001t0001g0089a0001c0001t0005g0246a0001c0001t0005g0280others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.67+17721G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157091 | ||||||
| chr11:35157105
|
G | A | 1 | a0001c0001t0004g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.67+17735G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157105 | ||||||
| chr11:35157162
|
A | T | 48 | a0001c0001t0001g0089a0001c0001t0005g0246a0001c0001t0005g0280others(45): Show | 51 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+17792A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157162 | ||||||
| chr11:35157242
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67+17872T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157242 | ||||||
| chr11:35157253
|
T | G | 48 | a0001c0001t0001g0089a0001c0001t0005g0246a0001c0001t0005g0280others(45): Show | 51 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+17883T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157253 | ||||||
| chr11:35157271
|
C | T | 1 | a0001c0002t0029g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+17901C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157271 | ||||||
| chr11:35157309
|
A | ATCTG | 5 | a0001c0001t0004g0004a0001c0001t0006g0168a0001c0001t0012g0005others(2): Show | 7 | HG02451.hp2 HG02809.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+17951_67+17954d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157309 | |||||
| chr11:35157321
|
G | GTCTA | 153 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0069others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.67+17994_67+17997d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
G | GTCTATCT others(1): Show |
12 | a0001c0001t0001g0201a0001c0001t0002g0010a0001c0001t0002g0061others(9): Show | 13 | HG00733.hp1 HG01074.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+17990_67+17997d others(10): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
G | GTCTATCT others(5): Show |
2 | a0001c0001t0005g0170a0001c0008t0002g0347 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.67+17959_67+17960i others(14): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
G | GTCTATCT others(5): Show |
1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.67+17986_67+17997d others(14): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
GTCTA | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(37): Show | 43 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.67+17994_67+17997d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
GTCTATCT others(1): Show |
G | 7 | a0001c0001t0001g0174a0001c0001t0001g0315a0001c0001t0002g0220others(4): Show | 7 | HG01070.hp1 HG01257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+17990_67+17997d others(10): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157321
|
GTCTATCT others(5): Show |
G | 19 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0254others(16): Show | 19 | HG00544.hp1 HG01071.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+17986_67+17997d others(14): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35157321 | |||||
| chr11:35157325
|
A | G | 10 | a0001c0001t0001g0048a0001c0001t0001g0175a0001c0001t0001g0240others(7): Show | 10 | HG00597.hp2 HG02109.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+17955A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157325 | ||||||
| chr11:35157329
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(29): Show | 34 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.67+17959A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157329 | ||||||
| chr11:35157333
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(24): Show | 29 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.67+17963A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157333 | ||||||
| chr11:35157337
|
A | G | 2 | a0001c0001t0001g0174a0001c0002t0006g0104 | 2 | HG01070.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.67+17967A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157337 | ||||||
| chr11:35157372
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67+18002G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157372 | ||||||
| chr11:35157454
|
T | C | 2 | a0001c0004t0007g0364a0001c0007t0002g0296 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.67+18084T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157454 | ||||||
| chr11:35157473
|
A | T | 1 | a0002c0003t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67+18103A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157473 | ||||||
| chr11:35157504
|
A | G | 1 | a0002c0005t0002g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.67+18134A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157504 | ||||||
| chr11:35157537
|
A | G | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.67+18167A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157537 | ||||||
| chr11:35157667
|
A | G | 2 | a0001c0001t0001g0113a0001c0004t0004g0119 | 2 | HG01928.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.67+18297A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35157667 | ||||||
| chr11:35158017
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.68-18558A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158017 | ||||||
| chr11:35158104
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(67): Show | 72 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.68-18471G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158104 | ||||||
| chr11:35158142
|
C | G | 19 | a0001c0001t0001g0089a0001c0001t0005g0307a0001c0001t0006g0304others(16): Show | 20 | HG00323.hp1 HG01243.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-18433C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158142 | ||||||
| chr11:35158355
|
C | T | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-18220C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158355 | ||||||
| chr11:35158356
|
G | A | 48 | a0001c0001t0001g0089a0001c0001t0005g0246a0001c0001t0005g0280others(45): Show | 51 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.68-18219G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158356 | ||||||
| chr11:35158706
|
C | T | 24 | a0001c0001t0001g0089a0001c0001t0005g0307a0001c0001t0006g0304others(21): Show | 25 | HG00323.hp1 HG01243.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.68-17869C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158706 | ||||||
| chr11:35158716
|
T | C | 2 | a0001c0004t0007g0364a0001c0007t0002g0296 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.68-17859T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158716 | ||||||
| chr11:35158719
|
T | C | 1 | a0001c0001t0009g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.68-17856T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158719 | ||||||
| chr11:35158730
|
A | G | 2 | a0001c0004t0007g0364a0001c0007t0002g0296 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.68-17845A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158730 | ||||||
| chr11:35158734
|
C | T | 2 | a0001c0004t0007g0364a0001c0007t0002g0296 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.68-17841C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158734 | ||||||
| chr11:35158759
|
T | C | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-17816T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158759 | ||||||
| chr11:35158770
|
G | T | 2 | a0001c0004t0007g0364a0001c0007t0002g0296 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.68-17805G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158770 | ||||||
| chr11:35158865
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.68-17710C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158865 | ||||||
| chr11:35158944
|
C | T | 1 | a0001c0001t0008g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.68-17631C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158944 | ||||||
| chr11:35158969
|
G | A | 4 | a0001c0004t0019g0054a0001c0008t0002g0347a0001c0008t0014g0172others(1): Show | 4 | HG03209.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-17606G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35158969 | ||||||
| chr11:35159047
|
A | G | 1 | a0001c0004t0019g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.68-17528A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159047 | ||||||
| chr11:35159141
|
T | C | 34 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0209others(31): Show | 35 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-17434T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159141 | ||||||
| chr11:35159513
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.68-17062C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159513 | ||||||
| chr11:35159715
|
C | T | 1 | a0001c0002t0006g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-16860C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159715 | ||||||
| chr11:35159740
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-16835G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159740 | ||||||
| chr11:35159755
|
G | A | 1 | a0001c0001t0013g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-16820G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159755 | ||||||
| chr11:35159982
|
T | C | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-16593T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35159982 | ||||||
| chr11:35160029
|
C | T | 1 | a0001c0001t0016g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68-16546C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160029 | ||||||
| chr11:35160066
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(202): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.68-16509T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160066 | ||||||
| chr11:35160132
|
C | G | 79 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(76): Show | 81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.68-16443C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160132 | ||||||
| chr11:35160349
|
C | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0004g0198others(1): Show | 4 | HG02615.hp2 NA18952.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-16226C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160349 | ||||||
| chr11:35160349
|
C | T | 6 | a0001c0001t0021g0091a0004c0009t0002g0186a0004c0009t0002g0300others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-16226C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160349 | ||||||
| chr11:35160445
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.68-16130C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160445 | ||||||
| chr11:35160446
|
G | A | 3 | a0001c0004t0019g0054a0001c0008t0014g0172a0001c0019t0030g0350 | 3 | HG03209.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-16129G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160446 | ||||||
| chr11:35160644
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.68-15931C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160644 | ||||||
| chr11:35160995
|
A | G | 20 | a0001c0001t0001g0089a0001c0001t0005g0307a0001c0001t0006g0304others(17): Show | 21 | HG00323.hp1 HG01099.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.68-15580A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35160995 | ||||||
| chr11:35161113
|
G | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(99): Show | 105 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.68-15462G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161113 | ||||||
| chr11:35161291
|
T | A | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-15284T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161291 | ||||||
| chr11:35161459
|
C | T | 2 | a0002c0005t0002g0263a0002c0005t0002g0264 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.68-15116C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161459 | ||||||
| chr11:35161472
|
G | A | 113 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(110): Show | 116 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.68-15103G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161472 | ||||||
| chr11:35161487
|
G | A | 3 | a0001c0004t0019g0054a0001c0008t0014g0172a0001c0019t0030g0350 | 3 | HG03209.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-15088G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161487 | ||||||
| chr11:35161492
|
C | G | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-15083C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161492 | ||||||
| chr11:35161502
|
G | A | 5 | a0001c0004t0007g0364a0001c0004t0019g0054a0001c0007t0002g0296others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-15073G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161502 | ||||||
| chr11:35161518
|
G | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(19): Show | 23 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-15057G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161518 | ||||||
| chr11:35161568
|
C | T | 6 | a0001c0001t0005g0307a0001c0001t0006g0304a0001c0002t0001g0306others(3): Show | 6 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-15007C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161568 | ||||||
| chr11:35161650
|
A | G | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-14925A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161650 | ||||||
| chr11:35161899
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-14676A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161899 | ||||||
| chr11:35161918
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.68-14657T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35161918 | ||||||
| chr11:35162030
|
T | G | 66 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(63): Show | 68 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.68-14545T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162030 | ||||||
| chr11:35162102
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.68-14473G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162102 | ||||||
| chr11:35162129
|
G | A | 5 | a0001c0004t0007g0364a0001c0004t0019g0054a0001c0007t0002g0296others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-14446G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162129 | ||||||
| chr11:35162206
|
T | C | 1 | a0001c0001t0022g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.68-14369T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162206 | ||||||
| chr11:35162264
|
G | GT | 22 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(19): Show | 23 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-14309dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35162264 | |||||
| chr11:35162291
|
T | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.68-14284T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162291 | ||||||
| chr11:35162308
|
T | A | 1 | a0001c0001t0037g0316 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.68-14267T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162308 | ||||||
| chr11:35162507
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.68-14068G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162507 | ||||||
| chr11:35162516
|
T | A | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-14059T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162516 | ||||||
| chr11:35162602
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.68-13973G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162602 | ||||||
| chr11:35162624
|
G | A | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-13951G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162624 | ||||||
| chr11:35162817
|
T | G | 123 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.68-13758T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162817 | ||||||
| chr11:35162887
|
C | T | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-13688C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162887 | ||||||
| chr11:35162894
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.68-13681G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162894 | ||||||
| chr11:35162933
|
C | G | 1 | a0001c0001t0001g0345 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.68-13642C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162933 | ||||||
| chr11:35162980
|
C | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(107): Show | 113 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.68-13595C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35162980 | ||||||
| chr11:35163005
|
A | T | 65 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(62): Show | 67 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.68-13570A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163005 | ||||||
| chr11:35163145
|
T | C | 2 | a0001c0001t0001g0317a0001c0004t0003g0328 | 2 | HG00609.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.68-13430T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163145 | ||||||
| chr11:35163183
|
G | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(107): Show | 113 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.68-13392G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163183 | ||||||
| chr11:35163194
|
G | A | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-13381G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163194 | ||||||
| chr11:35163251
|
CT | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(63): Show | 68 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.68-13311delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35163251 | |||||
| chr11:35163276
|
G | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(201): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.68-13299G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163276 | ||||||
| chr11:35163388
|
T | C | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-13187T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163388 | ||||||
| chr11:35163451
|
A | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(37): Show | 43 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-13124A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163451 | ||||||
| chr11:35163464
|
A | G | 2 | a0001c0007t0011g0087a0001c0007t0011g0088 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.68-13111A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163464 | ||||||
| chr11:35163509
|
A | G | 317 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(314): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.68-13066A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163509 | ||||||
| chr11:35163747
|
A | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.68-12828A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163747 | ||||||
| chr11:35163831
|
G | A | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-12744G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163831 | ||||||
| chr11:35163941
|
A | G | 316 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(313): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.68-12634A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35163941 | ||||||
| chr11:35164002
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68-12573C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164002 | ||||||
| chr11:35164003
|
G | A | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-12572G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164003 | ||||||
| chr11:35164044
|
C | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(58): Show | 66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.68-12531C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164044 | ||||||
| chr11:35164156
|
T | C | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-12419T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164156 | ||||||
| chr11:35164172
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.68-12403G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164172 | ||||||
| chr11:35164260
|
TG | T | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-12311delG | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35164260 | |||||
| chr11:35164264
|
G | A | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-12311G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164264 | ||||||
| chr11:35164265
|
T | A | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-12310T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164265 | ||||||
| chr11:35164288
|
T | C | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-12287T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164288 | ||||||
| chr11:35164325
|
A | G | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-12250A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164325 | ||||||
| chr11:35164416
|
G | A | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-12159G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164416 | ||||||
| chr11:35164435
|
A | C | 8 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0238others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-12140A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164435 | ||||||
| chr11:35164504
|
C | T | 1 | a0001c0001t0007g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68-12071C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164504 | ||||||
| chr11:35164648
|
C | T | 1 | a0001c0001t0006g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-11927C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164648 | ||||||
| chr11:35164697
|
C | T | 1 | a0002c0003t0005g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.68-11878C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164697 | ||||||
| chr11:35164782
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.68-11793A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35164782 | ||||||
| chr11:35165046
|
G | A | 2 | a0001c0001t0003g0111a0001c0001t0004g0042 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.68-11529G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165046 | ||||||
| chr11:35165070
|
G | T | 4 | a0001c0001t0006g0168a0001c0001t0006g0304a0001c0001t0012g0005others(1): Show | 5 | HG02451.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-11505G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165070 | ||||||
| chr11:35165101
|
T | G | 6 | a0001c0001t0032g0279a0001c0004t0001g0249a0001c0004t0002g0270others(3): Show | 6 | HG00408.hp2 HG00673.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-11474T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165101 | ||||||
| chr11:35165260
|
T | G | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-11315T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165260 | ||||||
| chr11:35165302
|
G | A | 1 | a0002c0003t0010g0015 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-11273G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165302 | ||||||
| chr11:35165457
|
C | A | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-11118C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165457 | ||||||
| chr11:35165672
|
A | G | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-10903A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165672 | ||||||
| chr11:35165680
|
A | G | 8 | a0001c0001t0006g0006a0001c0001t0006g0191a0001c0001t0006g0192others(5): Show | 9 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-10895A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165680 | ||||||
| chr11:35165801
|
C | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.68-10774C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165801 | ||||||
| chr11:35165806
|
C | A | 1 | a0001c0001t0001g0318 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.68-10769C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165806 | ||||||
| chr11:35165827
|
C | G | 4 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0008t0002g0347others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10748C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165827 | ||||||
| chr11:35165859
|
T | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(58): Show | 66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.68-10716T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35165859 | ||||||
| chr11:35166001
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.68-10574A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166001 | ||||||
| chr11:35166021
|
T | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.68-10554T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166021 | ||||||
| chr11:35166234
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-10341T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166234 | ||||||
| chr11:35166366
|
C | T | 28 | a0001c0001t0001g0089a0001c0001t0005g0307a0001c0001t0006g0166others(25): Show | 29 | HG00323.hp1 HG01099.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-10209C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166366 | ||||||
| chr11:35166612
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.68-9963C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166612 | ||||||
| chr11:35166644
|
G | A | 100 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(97): Show | 103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.68-9931G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166644 | ||||||
| chr11:35166742
|
C | T | 80 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.68-9833C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166742 | ||||||
| chr11:35166960
|
G | C | 100 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0062others(97): Show | 102 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.68-9615G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166960 | ||||||
| chr11:35166995
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.68-9580G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35166995 | ||||||
| chr11:35167005
|
A | G | 5 | a0001c0001t0021g0091a0004c0009t0002g0186a0004c0009t0002g0300others(2): Show | 5 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-9570A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167005 | ||||||
| chr11:35167025
|
C | T | 18 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(15): Show | 18 | HG00408.hp1 HG00673.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-9550C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167025 | ||||||
| chr11:35167041
|
G | A | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-9534G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167041 | ||||||
| chr11:35167204
|
C | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(207): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.68-9371C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167204 | ||||||
| chr11:35167213
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.68-9362T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167213 | ||||||
| chr11:35167252
|
T | TTG | 38 | a0001c0001t0001g0052a0001c0001t0001g0158a0001c0001t0001g0190others(35): Show | 39 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-9305_68-9304dup others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35167252 | |||||
| chr11:35167272
|
T | G | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-9303T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167272 | ||||||
| chr11:35167375
|
G | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0004g0198 | 3 | NA18952.hp2 NA18987.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.68-9200G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167375 | ||||||
| chr11:35167490
|
G | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-9085G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167490 | ||||||
| chr11:35167541
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.68-9034A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167541 | ||||||
| chr11:35167568
|
C | T | 2 | a0001c0002t0001g0219a0002c0003t0009g0218 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-9007C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167568 | ||||||
| chr11:35167601
|
T | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-8974T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167601 | ||||||
| chr11:35167698
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(122): Show | 129 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.68-8877T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167698 | ||||||
| chr11:35167812
|
C | G | 6 | a0001c0001t0006g0006a0001c0001t0006g0191a0001c0001t0006g0192others(3): Show | 7 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-8763C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35167812 | ||||||
| chr11:35168026
|
T | C | 1 | a0001c0001t0003g0357 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.68-8549T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168026 | ||||||
| chr11:35168182
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0007g0260 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.68-8393C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168182 | ||||||
| chr11:35168184
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.68-8391C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168184 | ||||||
| chr11:35168641
|
C | T | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68-7934C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168641 | ||||||
| chr11:35168742
|
T | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(52): Show | 56 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.68-7833T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168742 | ||||||
| chr11:35168753
|
C | T | 105 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(102): Show | 106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.68-7822C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168753 | ||||||
| chr11:35168820
|
T | C | 6 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-7755T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168820 | ||||||
| chr11:35168847
|
T | G | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-7728T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168847 | ||||||
| chr11:35168902
|
T | C | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.68-7673T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168902 | ||||||
| chr11:35168919
|
A | C | 6 | a0001c0001t0002g0261a0001c0001t0006g0166a0001c0001t0007g0260others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-7656A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168919 | ||||||
| chr11:35168922
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-7653C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168922 | ||||||
| chr11:35168941
|
A | C | 1 | a0001c0004t0004g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-7634A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35168941 | ||||||
| chr11:35169030
|
A | G | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-7545A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169030 | ||||||
| chr11:35169095
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-7480C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169095 | ||||||
| chr11:35169109
|
T | C | 2 | a0002c0003t0001g0244a0002c0003t0001g0245 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.68-7466T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169109 | ||||||
| chr11:35169329
|
A | G | 95 | a0001c0001t0001g0048a0001c0001t0001g0150a0001c0001t0001g0151others(92): Show | 101 | HG00323.hp1 HG00408.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-7246A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169329 | ||||||
| chr11:35169358
|
T | A | 1 | a0001c0001t0002g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.68-7217T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169358 | ||||||
| chr11:35169392
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-7183C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169392 | ||||||
| chr11:35169413
|
AAC | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(169): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-7134_68-7133del others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35169413 | |||||
| chr11:35169413
|
AACACACA others(1): Show |
A | 28 | a0001c0001t0032g0279a0001c0004t0001g0249a0001c0004t0001g0271others(25): Show | 30 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-7140_68-7133del others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35169413 | |||||
| chr11:35169568
|
G | A | 3 | a0001c0004t0004g0058a0001c0004t0004g0059a0003c0018t0003g0060 | 3 | HG00639.hp2 HG00735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.68-7007G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169568 | ||||||
| chr11:35169671
|
G | A | 4 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(1): Show | 4 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-6904G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169671 | ||||||
| chr11:35169695
|
C | T | 2 | a0001c0001t0001g0204a0001c0011t0001g0008 | 3 | NA18965.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.68-6880C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169695 | ||||||
| chr11:35169734
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-6841C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169734 | ||||||
| chr11:35169898
|
C | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.68-6677C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35169898 | ||||||
| chr11:35170050
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68-6525T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170050 | ||||||
| chr11:35170112
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-6463C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170112 | ||||||
| chr11:35170144
|
C | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-6431C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170144 | ||||||
| chr11:35170197
|
G | C | 25 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(22): Show | 27 | HG01070.hp1 HG02109.hp2 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.68-6378G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170197 | ||||||
| chr11:35170235
|
G | T | 43 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(40): Show | 46 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-6340G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170235 | ||||||
| chr11:35170290
|
C | A | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.68-6285C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170290 | ||||||
| chr11:35170307
|
A | G | 1 | a0001c0004t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.68-6268A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170307 | ||||||
| chr11:35170396
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-6179T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170396 | ||||||
| chr11:35170567
|
G | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(51): Show | 55 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.68-6008G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170567 | ||||||
| chr11:35170577
|
C | T | 1 | a0002c0003t0027g0358 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68-5998C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170577 | ||||||
| chr11:35170578
|
G | A | 1 | a0001c0001t0007g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-5997G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170578 | ||||||
| chr11:35170667
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-5908G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170667 | ||||||
| chr11:35170732
|
A | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-5843A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170732 | ||||||
| chr11:35170879
|
T | C | 1 | a0002c0003t0009g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-5696T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35170879 | ||||||
| chr11:35171082
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(200): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.68-5493C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171082 | ||||||
| chr11:35171108
|
A | G | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5467A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171108 | ||||||
| chr11:35171162
|
C | T | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68-5413C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171162 | ||||||
| chr11:35171299
|
T | C | 1 | a0001c0001t0016g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68-5276T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171299 | ||||||
| chr11:35171355
|
G | C | 25 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(22): Show | 26 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-5220G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171355 | ||||||
| chr11:35171437
|
T | A | 1 | a0001c0004t0003g0328 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.68-5138T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171437 | ||||||
| chr11:35171479
|
C | T | 3 | a0001c0001t0002g0220a0001c0001t0002g0229a0002c0003t0002g0255 | 3 | HG02148.hp2 NA18971.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.68-5096C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171479 | ||||||
| chr11:35171581
|
A | G | 27 | a0001c0004t0001g0249a0001c0004t0001g0271a0001c0004t0001g0276others(24): Show | 29 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-4994A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171581 | ||||||
| chr11:35171584
|
A | C | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-4991A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171584 | ||||||
| chr11:35171647
|
T | C | 2 | a0002c0003t0009g0180a0002c0003t0009g0181 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-4928T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171647 | ||||||
| chr11:35171787
|
A | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-4788A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171787 | ||||||
| chr11:35171841
|
CA | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(34): Show | 41 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.68-4722delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35171841 | |||||
| chr11:35171996
|
C | G | 1 | a0002c0003t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-4579C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35171996 | ||||||
| chr11:35172007
|
A | G | 1 | a0002c0005t0004g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.68-4568A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35172007 | ||||||
| chr11:35172170
|
T | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(201): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.68-4405T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35172170 | ||||||
| chr11:35172440
|
A | G | 1 | a0004c0009t0017g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.68-4135A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35172440 | ||||||
| chr11:35172545
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0002g0033 | 3 | NA18939.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.68-4030G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35172545 | ||||||
| chr11:35172849
|
CA | C | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.68-3715delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35172849 | |||||
| chr11:35172893
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-3682G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35172893 | ||||||
| chr11:35173165
|
T | A | 1 | a0001c0001t0023g0021 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.68-3410T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173165 | ||||||
| chr11:35173180
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0002g0085 | 2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.68-3395C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173180 | ||||||
| chr11:35173388
|
G | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0085 | 2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.68-3187G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173388 | ||||||
| chr11:35173552
|
T | TC | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-3017dupC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35173552 | |||||
| chr11:35173596
|
T | C | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-2979T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173596 | ||||||
| chr11:35173610
|
T | C | 25 | a0001c0004t0001g0249a0001c0004t0001g0271a0001c0004t0001g0276others(22): Show | 27 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-2965T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173610 | ||||||
| chr11:35173700
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.68-2875T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173700 | ||||||
| chr11:35173727
|
C | T | 2 | a0001c0001t0007g0107a0001c0001t0009g0105 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.68-2848C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173727 | ||||||
| chr11:35173728
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-2847G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173728 | ||||||
| chr11:35173875
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-2700T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173875 | ||||||
| chr11:35173947
|
C | A | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2628C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173947 | ||||||
| chr11:35173952
|
T | A | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2623T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173952 | ||||||
| chr11:35173953
|
A | G | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2622A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173953 | ||||||
| chr11:35173955
|
G | T | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2620G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173955 | ||||||
| chr11:35173956
|
A | C | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2619A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173956 | ||||||
| chr11:35173961
|
G | T | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2614G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173961 | ||||||
| chr11:35173962
|
G | T | 1 | a0008c0020t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.68-2613G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35173962 | ||||||
| chr11:35174008
|
AATAC | A | 5 | a0001c0001t0001g0234a0001c0001t0010g0232a0001c0010t0033g0187others(2): Show | 5 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-2555_68-2552del others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35174008 | |||||
| chr11:35174161
|
G | C | 1 | a0001c0001t0004g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.68-2414G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174161 | ||||||
| chr11:35174269
|
A | G | 1 | a0001c0001t0002g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.68-2306A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174269 | ||||||
| chr11:35174394
|
G | C | 63 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(60): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.68-2181G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174394 | ||||||
| chr11:35174429
|
T | C | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-2146T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174429 | ||||||
| chr11:35174438
|
G | A | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-2137G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174438 | ||||||
| chr11:35174522
|
G | A | 20 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(17): Show | 21 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.68-2053G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174522 | ||||||
| chr11:35174529
|
A | G | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-2046A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174529 | ||||||
| chr11:35174677
|
C | T | 1 | a0001c0001t0001g0366 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.68-1898C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174677 | ||||||
| chr11:35174730
|
A | G | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68-1845A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174730 | ||||||
| chr11:35174792
|
G | A | 6 | a0001c0001t0006g0006a0001c0001t0006g0191a0001c0001t0006g0192others(3): Show | 7 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-1783G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174792 | ||||||
| chr11:35174844
|
T | C | 1 | a0001c0001t0022g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.68-1731T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174844 | ||||||
| chr11:35174864
|
A | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-1711A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174864 | ||||||
| chr11:35174890
|
C | T | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-1685C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174890 | ||||||
| chr11:35174998
|
G | A | 1 | a0001c0001t0034g0120 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.68-1577G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35174998 | ||||||
| chr11:35175044
|
TG | T | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-1530delG | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175044 | ||||||
| chr11:35175052
|
C | T | 54 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(51): Show | 55 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.68-1523C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175052 | ||||||
| chr11:35175053
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.68-1522G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175053 | ||||||
| chr11:35175073
|
G | C | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-1502G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175073 | ||||||
| chr11:35175273
|
T | C | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-1302T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175273 | ||||||
| chr11:35175283
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0110a0002c0003t0001g0112 | 3 | HG00738.hp1 HG02258.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.68-1292A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175283 | ||||||
| chr11:35175324
|
C | G | 1 | a0001c0001t0002g0348 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.68-1251C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175324 | ||||||
| chr11:35175398
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-1177G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175398 | ||||||
| chr11:35175732
|
T | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-843T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175732 | ||||||
| chr11:35175828
|
A | G | 1 | a0001c0004t0001g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-747A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175828 | ||||||
| chr11:35175830
|
C | T | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-745C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35175830 | ||||||
| chr11:35175864
|
C | CT | 25 | a0001c0001t0001g0069a0001c0001t0001g0147a0001c0001t0001g0150others(22): Show | 25 | HG01074.hp2 HG01099.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-692dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35175864 | |||||
| chr11:35175864
|
CT | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(27): Show | 32 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-692delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35175864 | |||||
| chr11:35175864
|
CTTT | C | 11 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0006g0360others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-694_68-692delTT others(1): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35175864 | |||||
| chr11:35175864
|
CTTTT | C | 7 | a0001c0001t0005g0189a0001c0001t0005g0307a0001c0002t0001g0306others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-695_68-692delTT others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35175864 | |||||
| chr11:35176039
|
A | AT | 23 | a0001c0001t0001g0086a0001c0001t0001g0234a0001c0001t0001g0254others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-515dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176039
|
AT | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0065others(67): Show | 71 | HG00544.hp2 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-515delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176039
|
ATT | A | 15 | a0001c0001t0002g0261a0001c0001t0006g0006a0001c0001t0006g0166others(12): Show | 17 | HG00738.hp2 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.68-516_68-515delTT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176039
|
ATTTTTTT | A | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.68-521_68-515delTT others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176039
|
ATTTTTTT others(2): Show |
A | 26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-523_68-515delTT others(7): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176039
|
ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0005g0307a0001c0002t0001g0306a0001c0002t0007g0012others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-526_68-515delTT others(10): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 35176039 | |||||
| chr11:35176100
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.68-475T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176100 | ||||||
| chr11:35176154
|
T | C | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-421T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176154 | ||||||
| chr11:35176253
|
A | G | 1 | a0001c0004t0019g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.68-322A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176253 | ||||||
| chr11:35176442
|
T | C | 25 | a0001c0004t0001g0249a0001c0004t0001g0271a0001c0004t0001g0276others(22): Show | 27 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.68-133T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176442 | ||||||
| chr11:35176460
|
G | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(51): Show | 55 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.68-115G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176460 | ||||||
| chr11:35176485
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.68-90A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176485 | ||||||
| chr11:35176561
|
A | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(199): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.68-14A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 1/17 | chr11 | 35176561 | ||||||
| chr11:35176791
|
GC | G | 8 | a0001c0001t0001g0034a0001c0001t0001g0204a0001c0001t0001g0236others(5): Show | 9 | HG00597.hp2 HG00609.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+52delC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35176791 | ||||||
| chr11:35176857
|
C | T | 1 | a0004c0009t0017g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.233+117C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35176857 | ||||||
| chr11:35176947
|
C | T | 2 | a0001c0004t0004g0018a0005c0013t0003g0017 | 2 | HG00323.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.233+207C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35176947 | ||||||
| chr11:35177114
|
T | C | 15 | a0001c0001t0002g0261a0001c0001t0006g0006a0001c0001t0006g0166others(12): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.233+374T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177114 | ||||||
| chr11:35177154
|
CTACTCTC others(3): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.233+427_233+436del others(10): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 35177154 | |||||
| chr11:35177176
|
A | G | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+436A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177176 | ||||||
| chr11:35177183
|
A | T | 19 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.233+443A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177183 | ||||||
| chr11:35177183
|
AT | A | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.233+451delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 35177183 | |||||
| chr11:35177202
|
CTA | C | 11 | a0001c0001t0002g0125a0001c0001t0002g0206a0001c0001t0002g0220others(8): Show | 11 | HG00544.hp1 HG02027.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+464_233+465del others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 35177202 | |||||
| chr11:35177305
|
C | T | 26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.233+565C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177305 | ||||||
| chr11:35177315
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0002g0085 | 2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.233+575A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177315 | ||||||
| chr11:35177361
|
T | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.233+621T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177361 | ||||||
| chr11:35177413
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.233+673C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177413 | ||||||
| chr11:35177687
|
G | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(307): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.233+947G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177687 | ||||||
| chr11:35177892
|
G | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.233+1152G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35177892 | ||||||
| chr11:35178053
|
G | A | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.233+1313G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178053 | ||||||
| chr11:35178333
|
A | G | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.233+1593A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178333 | ||||||
| chr11:35178376
|
G | A | 26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.233+1636G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178376 | ||||||
| chr11:35178429
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0325a0001c0001t0002g0290 | 3 | NA18973.hp2 NA18988.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.233+1689G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178429 | ||||||
| chr11:35178493
|
G | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(6): Show | 9 | HG01070.hp1 HG03927.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+1753G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178493 | ||||||
| chr11:35178665
|
G | T | 4 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0008t0002g0347others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1609G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178665 | ||||||
| chr11:35178722
|
A | C | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.234-1552A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178722 | ||||||
| chr11:35178780
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(300): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.234-1494T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178780 | ||||||
| chr11:35178930
|
A | G | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234-1344A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35178930 | ||||||
| chr11:35179021
|
T | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(7): Show | 10 | HG01070.hp1 HG03927.hp2 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.234-1253T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179021 | ||||||
| chr11:35179085
|
T | C | 1 | a0002c0003t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234-1189T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179085 | ||||||
| chr11:35179126
|
A | G | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-1148A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179126 | ||||||
| chr11:35179369
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(75): Show | 81 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.234-905G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179369 | ||||||
| chr11:35179381
|
C | A | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.234-893C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179381 | ||||||
| chr11:35179483
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.234-791G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179483 | ||||||
| chr11:35179587
|
G | A | 1 | a0001c0001t0015g0043 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.234-687G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179587 | ||||||
| chr11:35179737
|
T | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234-537T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179737 | ||||||
| chr11:35179968
|
T | G | 7 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0004g0119others(4): Show | 9 | HG01255.hp2 HG01346.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.234-306T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179968 | ||||||
| chr11:35179983
|
C | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.234-291C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35179983 | ||||||
| chr11:35180029
|
AT | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(26): Show | 31 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.234-236delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 35180029 | |||||
| chr11:35180263
|
T | C | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.234-11T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 2/17 | chr11 | 35180263 | ||||||
| chr11:35180411
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0031g0126 | 2 | HG03704.hp2 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.367+4G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180411 | ||||||
| chr11:35180414
|
T | C | 1 | a0001c0004t0019g0054 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.367+7T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180414 | ||||||
| chr11:35180435
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.367+28C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180435 | ||||||
| chr11:35180556
|
A | G | 3 | a0001c0001t0001g0318a0001c0001t0001g0343a0002c0003t0004g0057 | 3 | HG01952.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.367+149A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180556 | ||||||
| chr11:35180590
|
A | G | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.367+183A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180590 | ||||||
| chr11:35180647
|
G | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0254a0001c0001t0001g0292others(3): Show | 6 | HG01071.hp2 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+240G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180647 | ||||||
| chr11:35180740
|
A | C | 1 | a0001c0001t0001g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.367+333A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180740 | ||||||
| chr11:35180768
|
T | C | 17 | a0001c0001t0001g0122a0001c0001t0001g0254a0001c0001t0001g0292others(14): Show | 17 | HG00544.hp1 HG01071.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.367+361T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180768 | ||||||
| chr11:35180813
|
A | G | 1 | a0001c0001t0005g0339 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367+406A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180813 | ||||||
| chr11:35180877
|
G | T | 45 | a0001c0004t0001g0068a0001c0004t0001g0249a0001c0004t0001g0271others(42): Show | 48 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.367+470G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180877 | ||||||
| chr11:35180950
|
G | A | 1 | a0001c0001t0016g0155 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.367+543G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35180950 | ||||||
| chr11:35181213
|
C | T | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.367+806C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181213 | ||||||
| chr11:35181399
|
T | A | 15 | a0001c0001t0002g0261a0001c0001t0006g0006a0001c0001t0006g0166others(12): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.367+992T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181399 | ||||||
| chr11:35181491
|
C | T | 5 | a0001c0001t0005g0307a0001c0002t0001g0306a0001c0002t0007g0012others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+1084C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181491 | ||||||
| chr11:35181546
|
G | A | 3 | a0001c0001t0001g0113a0002c0003t0011g0127a0002c0003t0011g0128 | 3 | HG01070.hp2 HG01071.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.367+1139G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181546 | ||||||
| chr11:35181668
|
A | G | 1 | a0001c0002t0005g0361 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.367+1261A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181668 | ||||||
| chr11:35181669
|
C | CATATATA others(53): Show |
1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.367+1300_367+1301i others(62): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181669 | |||||
| chr11:35181670
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0019g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.367+1279_367+1290d others(14): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181670 | |||||
| chr11:35181672
|
A | ATATATAT others(19): Show |
7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+1280_367+1305d others(28): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181672 | |||||
| chr11:35181680
|
A | ATT | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.367+1275_367+1276d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181680 | |||||
| chr11:35181743
|
C | T | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+1336C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181743 | ||||||
| chr11:35181758
|
ATATTTAT others(25): Show |
A | 6 | a0001c0004t0013g0003a0001c0007t0002g0099a0001c0007t0002g0301others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+1355_367+1386d others(34): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181758 | |||||
| chr11:35181778
|
A | C | 9 | a0001c0001t0006g0006a0001c0001t0006g0168a0001c0001t0006g0191others(6): Show | 11 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.367+1371A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181778 | ||||||
| chr11:35181790
|
T | TTA | 86 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(83): Show | 90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.367+1390_367+1391d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181790 | |||||
| chr11:35181858
|
AATTT | A | 26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.367+1454_367+1457d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181858 | |||||
| chr11:35181861
|
TTA | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.367+1466_367+1467d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181861 | |||||
| chr11:35181866
|
T | TATATATT others(34): Show |
1 | a0002c0005t0001g0269 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.367+1465_367+1466i others(43): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181866 | |||||
| chr11:35181881
|
TA | T | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+1476delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181881 | |||||
| chr11:35181885
|
TC | T | 44 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0150others(41): Show | 45 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.367+1479delC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181885 | ||||||
| chr11:35181886
|
C | CATA | 5 | a0001c0007t0005g0185a0001c0007t0011g0087a0001c0007t0011g0088others(2): Show | 5 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+1479_367+1480i others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181886 | ||||||
| chr11:35181886
|
C | CATATATA others(39): Show |
39 | a0001c0001t0032g0279a0001c0004t0001g0068a0001c0004t0001g0249others(36): Show | 42 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.367+1479_367+1480i others(48): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181886 | ||||||
| chr11:35181886
|
C | CATATATA others(41): Show |
1 | a0001c0007t0002g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+1479_367+1480i others(50): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181886 | ||||||
| chr11:35181898
|
TA | T | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.367+1493delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181898 | |||||
| chr11:35181907
|
A | T | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.367+1500A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181907 | ||||||
| chr11:35181909
|
ATATATTA others(5): Show |
A | 2 | a0001c0007t0011g0087a0001c0007t0011g0088 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.367+1515_367+1526d others(14): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181909 | |||||
| chr11:35181913
|
A | ATTATAT | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+1507_367+1512d others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181913 | |||||
| chr11:35181920
|
A | ATT | 26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.367+1514_367+1515d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181920 | |||||
| chr11:35181920
|
A | T | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+1513A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181920 | ||||||
| chr11:35181921
|
T | A | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+1514T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181921 | ||||||
| chr11:35181921
|
T | TAAATATA others(43): Show |
2 | a0001c0002t0001g0219a0002c0003t0009g0218 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.367+1514_367+1515i others(52): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181921 | ||||||
| chr11:35181921
|
T | TAATTCAT others(31): Show |
1 | a0001c0004t0007g0364 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.367+1514_367+1515i others(40): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181921 | ||||||
| chr11:35181921
|
T | TTA | 69 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(66): Show | 74 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.367+1518_367+1519d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181921 | |||||
| chr11:35181921
|
T | TTATATAT others(50): Show |
37 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(34): Show | 38 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.367+1519_367+1520i others(59): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181921 | |||||
| chr11:35181921
|
T | TTATATAT others(81): Show |
5 | a0001c0001t0006g0176a0001c0001t0006g0177a0001c0002t0005g0101others(2): Show | 5 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+1519_367+1520i others(90): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181921 | |||||
| chr11:35181926
|
T | A | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+1519T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181926 | ||||||
| chr11:35181926
|
T | TA | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1519_367+1520i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181926 | ||||||
| chr11:35181926
|
T | TATTATAA others(70): Show |
6 | a0001c0001t0005g0307a0001c0002t0001g0306a0001c0002t0007g0012others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.367+1519_367+1520i others(79): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181926 | ||||||
| chr11:35181927
|
T | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(30): Show | 35 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.367+1520T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181927 | ||||||
| chr11:35181928
|
A | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(24): Show | 29 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.367+1521A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181928 | ||||||
| chr11:35181929
|
T | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1522T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181929 | ||||||
| chr11:35181934
|
A | AG | 14 | a0001c0001t0002g0250a0001c0001t0005g0307a0001c0001t0007g0094others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.367+1527_367+1528i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181934 | ||||||
| chr11:35181934
|
A | AT | 27 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(24): Show | 29 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.367+1527_367+1528i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181934 | ||||||
| chr11:35181934
|
A | ATTATATA others(28): Show |
12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+1527_367+1528i others(37): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181934 | ||||||
| chr11:35181935
|
A | G | 1 | a0002c0003t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367+1528A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181935 | ||||||
| chr11:35181935
|
A | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1528A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181935 | ||||||
| chr11:35181936
|
AT | A | 44 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(41): Show | 45 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.367+1531delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181936 | |||||
| chr11:35181945
|
A | AAT | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.367+1546_367+1547d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181945 | |||||
| chr11:35181945
|
A | T | 11 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(8): Show | 11 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.367+1538A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181945 | ||||||
| chr11:35181946
|
A | ATATATAT others(28): Show |
26 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(23): Show | 27 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.367+1553_367+1587d others(37): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181946 | |||||
| chr11:35181950
|
A | AT | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1544dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181950 | |||||
| chr11:35181955
|
A | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1548A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181955 | ||||||
| chr11:35181957
|
T | TA | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1550_367+1551i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181957 | ||||||
| chr11:35181958
|
T | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1551T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181958 | ||||||
| chr11:35181959
|
T | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1552T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181959 | ||||||
| chr11:35181966
|
TA | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1560delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181966 | ||||||
| chr11:35181970
|
A | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1563A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181970 | ||||||
| chr11:35181971
|
A | G | 2 | a0001c0007t0005g0185a0001c0019t0030g0350 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.367+1564A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181971 | ||||||
| chr11:35181971
|
ATAT | A | 12 | a0001c0001t0001g0135a0001c0001t0002g0124a0001c0001t0002g0148others(9): Show | 12 | HG02071.hp2 HG02080.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+1568_367+1570d others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181971 | |||||
| chr11:35181993
|
T | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1586T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35181993 | ||||||
| chr11:35181997
|
A | ATAATATA others(7): Show |
8 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1591_367+1592i others(16): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35181997 | |||||
| chr11:35182004
|
T | TATATTTA others(23): Show |
1 | a0001c0004t0004g0018 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.367+1601_367+1602i others(32): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35182004 | |||||
| chr11:35182008
|
T | TAAATA | 8 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1601_367+1602i others(7): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182008 | ||||||
| chr11:35182009
|
G | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(199): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.367+1602G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182009 | ||||||
| chr11:35182016
|
TG | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1610delG | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182016 | ||||||
| chr11:35182026
|
A | AATTTAT | 8 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1621_367+1622i others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35182026 | |||||
| chr11:35182029
|
A | ATATATAA others(53): Show |
1 | a0001c0001t0004g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.367+1626_367+1627i others(62): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35182029 | |||||
| chr11:35182029
|
A | T | 8 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1622A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182029 | ||||||
| chr11:35182034
|
C | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1627C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182034 | ||||||
| chr11:35182036
|
C | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0256a0001c0001t0002g0266others(6): Show | 9 | HG00733.hp1 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1629C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182036 | ||||||
| chr11:35182120
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.367+1713G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182120 | ||||||
| chr11:35182164
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+1757C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182164 | ||||||
| chr11:35182214
|
A | C | 7 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0007g0169others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+1807A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182214 | ||||||
| chr11:35182353
|
T | G | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.367+1946T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182353 | ||||||
| chr11:35182415
|
G | A | 1 | a0001c0002t0038g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367+2008G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182415 | ||||||
| chr11:35182420
|
A | G | 15 | a0001c0001t0002g0261a0001c0001t0006g0006a0001c0001t0006g0166others(12): Show | 17 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.367+2013A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182420 | ||||||
| chr11:35182459
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.367+2052C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182459 | ||||||
| chr11:35182575
|
A | G | 2 | a0001c0001t0003g0111a0001c0001t0004g0042 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.367+2168A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182575 | ||||||
| chr11:35182704
|
G | C | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.367+2297G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182704 | ||||||
| chr11:35182800
|
G | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.367+2393G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182800 | ||||||
| chr11:35182969
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.367+2562G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35182969 | ||||||
| chr11:35183148
|
C | T | 1 | a0001c0004t0003g0328 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.367+2741C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35183148 | ||||||
| chr11:35183338
|
C | CA | 136 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0052others(133): Show | 141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.367+2944dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35183338 | |||||
| chr11:35183338
|
C | CAA | 7 | a0001c0001t0005g0307a0001c0002t0001g0306a0001c0002t0007g0012others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+2943_367+2944d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35183338 | |||||
| chr11:35183338
|
CA | C | 28 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(25): Show | 30 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.367+2944delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35183338 | |||||
| chr11:35183474
|
A | T | 6 | a0001c0001t0005g0307a0001c0002t0001g0306a0001c0002t0007g0012others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.367+3067A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35183474 | ||||||
| chr11:35183490
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.367+3083A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35183490 | ||||||
| chr11:35183537
|
C | T | 1 | a0002c0003t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367+3130C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35183537 | ||||||
| chr11:35183854
|
G | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-2978G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35183854 | ||||||
| chr11:35184105
|
G | A | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368-2727G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184105 | ||||||
| chr11:35184136
|
G | T | 1 | a0001c0001t0019g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.368-2696G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184136 | ||||||
| chr11:35184171
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0004g0109a0001c0001t0004g0146 | 3 | HG00280.hp1 HG01261.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.368-2661C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184171 | ||||||
| chr11:35184288
|
T | C | 28 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(25): Show | 29 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.368-2544T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184288 | ||||||
| chr11:35184289
|
C | T | 28 | a0001c0001t0001g0048a0001c0001t0001g0201a0001c0001t0001g0208others(25): Show | 29 | HG00621.hp2 HG01891.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.368-2543C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184289 | ||||||
| chr11:35184343
|
C | T | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.368-2489C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184343 | ||||||
| chr11:35184414
|
A | G | 1 | a0002c0003t0039g0216 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.368-2418A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184414 | ||||||
| chr11:35184428
|
G | C | 1 | a0002c0003t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.368-2404G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184428 | ||||||
| chr11:35184498
|
G | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-2334G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184498 | ||||||
| chr11:35184728
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.368-2104A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184728 | ||||||
| chr11:35184742
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.368-2090G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184742 | ||||||
| chr11:35184747
|
T | A | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.368-2085T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184747 | ||||||
| chr11:35184857
|
TTTAGGGG others(9): Show |
T | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.368-1969_368-1954d others(18): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35184857 | |||||
| chr11:35184878
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0062others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.368-1954G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184878 | ||||||
| chr11:35184937
|
A | G | 2 | a0001c0001t0001g0086a0002c0003t0001g0112 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.368-1895A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35184937 | ||||||
| chr11:35185308
|
A | G | 1 | a0001c0004t0001g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.368-1524A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35185308 | ||||||
| chr11:35185332
|
G | A | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-1500G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35185332 | ||||||
| chr11:35185507
|
C | T | 1 | a0001c0004t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.368-1325C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35185507 | ||||||
| chr11:35185572
|
T | TCCTC | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.368-1251_368-1248d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35185572 | |||||
| chr11:35185581
|
CCTCT | C | 18 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0005g0189others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-1247_368-1244d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35185581 | |||||
| chr11:35185769
|
T | G | 1 | a0001c0001t0003g0207 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.368-1063T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35185769 | ||||||
| chr11:35185937
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(42): Show | 47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.368-895G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35185937 | ||||||
| chr11:35186043
|
C | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(6): Show | 9 | HG01070.hp1 HG03927.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.368-789C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35186043 | ||||||
| chr11:35186054
|
GA | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(198): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.368-768delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35186054 | |||||
| chr11:35186188
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(198): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.368-644C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35186188 | ||||||
| chr11:35186519
|
CTA | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(21): Show | 26 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.368-311_368-310del others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | 35186519 | |||||
| chr11:35186521
|
A | T | 1 | a0001c0001t0004g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.368-311A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35186521 | ||||||
| chr11:35186573
|
A | G | 1 | a0001c0002t0002g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368-259A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35186573 | ||||||
| chr11:35186704
|
A | G | 82 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(79): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.368-128A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 3/17 | chr11 | 35186704 | ||||||
| chr11:35186966
|
T | C | 1 | a0001c0002t0038g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436+66T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35186966 | ||||||
| chr11:35187091
|
G | A | 47 | a0001c0001t0002g0032a0001c0001t0006g0168a0001c0004t0001g0068others(44): Show | 50 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.436+191G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187091 | ||||||
| chr11:35187177
|
G | A | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0174others(7): Show | 10 | HG01070.hp1 HG03927.hp2 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+277G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187177 | ||||||
| chr11:35187402
|
C | T | 1 | a0001c0007t0002g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.436+502C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187402 | ||||||
| chr11:35187446
|
T | C | 1 | a0001c0001t0031g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.436+546T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187446 | ||||||
| chr11:35187739
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436+839G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187739 | ||||||
| chr11:35187755
|
G | C | 1 | a0004c0009t0017g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.436+855G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187755 | ||||||
| chr11:35187822
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.436+922C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35187822 | ||||||
| chr11:35188037
|
A | G | 17 | a0001c0001t0001g0048a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 17 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.436+1137A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188037 | ||||||
| chr11:35188040
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.436+1140A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188040 | ||||||
| chr11:35188082
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.436+1182C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188082 | ||||||
| chr11:35188303
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.436+1403C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188303 | ||||||
| chr11:35188532
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.437-1303G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188532 | ||||||
| chr11:35188570
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-1265G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188570 | ||||||
| chr11:35188711
|
G | A | 2 | a0001c0001t0003g0312a0001c0001t0003g0319 | 2 | HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.437-1124G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188711 | ||||||
| chr11:35188765
|
C | T | 1 | a0001c0001t0004g0157 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.437-1070C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35188765 | ||||||
| chr11:35189043
|
C | A | 1 | a0001c0001t0001g0351 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.437-792C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189043 | ||||||
| chr11:35189119
|
T | C | 1 | a0003c0006t0003g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.437-716T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189119 | ||||||
| chr11:35189135
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.437-700A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189135 | ||||||
| chr11:35189219
|
C | T | 5 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0002g0253others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-616C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189219 | ||||||
| chr11:35189227
|
G | A | 1 | a0001c0001t0001g0366 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.437-608G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189227 | ||||||
| chr11:35189251
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(238): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.437-584G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189251 | ||||||
| chr11:35189319
|
T | G | 209 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(206): Show | 213 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.437-516T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189319 | ||||||
| chr11:35189325
|
T | C | 1 | a0001c0001t0006g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437-510T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189325 | ||||||
| chr11:35189355
|
G | C | 1 | a0001c0001t0002g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.437-480G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189355 | ||||||
| chr11:35189556
|
T | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0240 | 2 | NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.437-279T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 4/17 | chr11 | 35189556 | ||||||
| chr11:35190442
|
T | G | 3 | a0001c0001t0001g0190a0001c0001t0005g0189a0001c0019t0030g0350 | 3 | HG01109.hp1 HG03239.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+377T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190442 | ||||||
| chr11:35190527
|
T | G | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.667+462T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190527 | ||||||
| chr11:35190537
|
T | G | 1 | a0001c0001t0025g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.667+472T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190537 | ||||||
| chr11:35190741
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(294): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.667+676A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190741 | ||||||
| chr11:35190817
|
G | A | 1 | a0001c0001t0005g0246 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.667+752G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190817 | ||||||
| chr11:35190839
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0005g0189 | 2 | HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.667+774T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190839 | ||||||
| chr11:35190897
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0005g0189a0001c0019t0030g0350 | 3 | HG01109.hp1 HG03239.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+832C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35190897 | ||||||
| chr11:35191073
|
C | T | 2 | a0001c0007t0011g0087a0001c0007t0011g0088 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.667+1008C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191073 | ||||||
| chr11:35191094
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.667+1029A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191094 | ||||||
| chr11:35191177
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.667+1112G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191177 | ||||||
| chr11:35191340
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0239a0001c0001t0016g0155 | 3 | NA18940.hp2 NA19065.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.667+1275C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191340 | ||||||
| chr11:35191403
|
T | C | 6 | a0001c0002t0006g0106a0001c0004t0013g0003a0001c0007t0002g0099others(3): Show | 7 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+1338T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191403 | ||||||
| chr11:35191495
|
G | A | 48 | a0001c0001t0001g0048a0001c0001t0001g0174a0001c0001t0002g0261others(45): Show | 50 | HG00733.hp2 HG01070.hp1 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.667+1430G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191495 | ||||||
| chr11:35191579
|
G | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(293): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.667+1514G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191579 | ||||||
| chr11:35191694
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0005g0189a0001c0019t0030g0350 | 3 | HG01109.hp1 HG03239.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+1629C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191694 | ||||||
| chr11:35191747
|
T | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.667+1682T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191747 | ||||||
| chr11:35191831
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.667+1766G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191831 | ||||||
| chr11:35191925
|
G | A | 1 | a0001c0004t0001g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.667+1860G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35191925 | ||||||
| chr11:35192108
|
T | G | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.667+2043T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35192108 | ||||||
| chr11:35192679
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0005g0189a0001c0019t0030g0350 | 3 | HG01109.hp1 HG03239.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+2614A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35192679 | ||||||
| chr11:35192790
|
CT | C | 59 | a0001c0001t0001g0048a0001c0001t0001g0174a0001c0001t0001g0338others(56): Show | 61 | HG00733.hp2 HG01070.hp1 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.667+2745delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 35192790 | |||||
| chr11:35192790
|
CTT | C | 206 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(203): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.667+2744_667+2745d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 35192790 | |||||
| chr11:35192796
|
T | C | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.667+2731T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35192796 | ||||||
| chr11:35192884
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0201a0001c0001t0002g0348others(1): Show | 4 | HG02040.hp1 HG02040.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+2819T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35192884 | ||||||
| chr11:35192888
|
C | A | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.667+2823C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35192888 | ||||||
| chr11:35193061
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.667+2996C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193061 | ||||||
| chr11:35193335
|
G | A | 1 | a0001c0002t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.667+3270G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193335 | ||||||
| chr11:35193347
|
C | A | 5 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0002g0253others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+3282C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193347 | ||||||
| chr11:35193561
|
G | A | 2 | a0001c0001t0002g0032a0002c0003t0003g0067 | 2 | HG00741.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.668-3185G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193561 | ||||||
| chr11:35193588
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0005g0189 | 2 | HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.668-3158A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193588 | ||||||
| chr11:35193912
|
A | G | 3 | a0001c0001t0004g0042a0001c0001t0004g0258a0001c0001t0014g0259 | 3 | HG00733.hp1 HG01123.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.668-2834A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35193912 | ||||||
| chr11:35194179
|
T | G | 209 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(206): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.668-2567T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194179 | ||||||
| chr11:35194377
|
T | C | 3 | a0001c0001t0006g0166a0001c0001t0008g0295a0001c0002t0012g0165 | 3 | HG02109.hp2 HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.668-2369T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194377 | ||||||
| chr11:35194450
|
C | T | 1 | a0001c0004t0007g0364 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.668-2296C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194450 | ||||||
| chr11:35194610
|
C | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0160a0001c0001t0001g0317others(19): Show | 23 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-2136C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194610 | ||||||
| chr11:35194722
|
T | A | 1 | a0001c0001t0006g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.668-2024T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194722 | ||||||
| chr11:35194769
|
A | G | 2 | a0001c0002t0001g0219a0002c0003t0009g0218 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.668-1977A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194769 | ||||||
| chr11:35194911
|
G | C | 5 | a0001c0001t0007g0169a0001c0002t0002g0184a0001c0002t0006g0104others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.668-1835G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35194911 | ||||||
| chr11:35195092
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.668-1654G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195092 | ||||||
| chr11:35195144
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.668-1602G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195144 | ||||||
| chr11:35195152
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.668-1594C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195152 | ||||||
| chr11:35195153
|
G | A | 32 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0145others(29): Show | 32 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.668-1593G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195153 | ||||||
| chr11:35195254
|
T | C | 3 | a0001c0001t0001g0234a0002c0003t0009g0218a0002c0003t0010g0233 | 3 | HG00099.hp2 HG00280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.668-1492T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195254 | ||||||
| chr11:35195267
|
A | G | 202 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(199): Show | 204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.668-1479A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195267 | ||||||
| chr11:35195353
|
G | A | 12 | a0001c0001t0001g0134a0001c0001t0006g0360a0001c0002t0002g0196others(9): Show | 12 | HG00733.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.668-1393G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195353 | ||||||
| chr11:35195388
|
C | T | 167 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(164): Show | 169 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.668-1358C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195388 | ||||||
| chr11:35195515
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.668-1231G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195515 | ||||||
| chr11:35195552
|
T | C | 1 | a0001c0001t0028g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.668-1194T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195552 | ||||||
| chr11:35195571
|
G | GA | 6 | a0001c0001t0002g0250a0001c0001t0007g0094a0001c0001t0007g0095others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-1166dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 35195571 | |||||
| chr11:35195686
|
A | G | 1 | a0001c0001t0006g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.668-1060A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195686 | ||||||
| chr11:35195816
|
C | T | 1 | a0001c0001t0006g0227 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.668-930C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195816 | ||||||
| chr11:35195859
|
C | A | 1 | a0001c0001t0028g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.668-887C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195859 | ||||||
| chr11:35195866
|
T | G | 7 | a0001c0001t0002g0063a0002c0003t0009g0179a0002c0003t0009g0180others(4): Show | 7 | HG00733.hp2 HG01358.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.668-880T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195866 | ||||||
| chr11:35195875
|
A | C | 1 | a0002c0003t0002g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.668-871A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35195875 | ||||||
| chr11:35196092
|
T | C | 40 | a0001c0002t0001g0219a0001c0002t0001g0306a0001c0002t0002g0014others(37): Show | 40 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.668-654T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35196092 | ||||||
| chr11:35196198
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(317): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.668-548T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35196198 | ||||||
| chr11:35196272
|
T | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0118others(2): Show | 6 | HG00597.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-474T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35196272 | ||||||
| chr11:35196330
|
G | A | 5 | a0001c0001t0002g0261a0001c0001t0005g0170a0001c0001t0005g0173others(2): Show | 5 | HG02258.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.668-416G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35196330 | ||||||
| chr11:35196445
|
G | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(36): Show | 42 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.668-301G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | chr11 | 35196445 | ||||||
| chr11:35196534
|
AT | A | 320 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(317): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.668-209delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 35196534 | |||||
| chr11:35196898
|
A | G | 4 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162others(1): Show | 4 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+24A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35196898 | ||||||
| chr11:35196979
|
A | T | 1 | a0001c0001t0003g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.796+105A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35196979 | ||||||
| chr11:35196995
|
A | G | 1 | a0001c0001t0025g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.796+121A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35196995 | ||||||
| chr11:35197016
|
C | A | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.796+142C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35197016 | ||||||
| chr11:35197120
|
C | T | 29 | a0001c0002t0001g0219a0001c0002t0001g0306a0001c0002t0002g0014others(26): Show | 29 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.796+246C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35197120 | ||||||
| chr11:35197483
|
G | A | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.796+609G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35197483 | ||||||
| chr11:35197598
|
T | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.797-523T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35197598 | ||||||
| chr11:35197625
|
C | T | 1 | a0001c0004t0019g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.797-496C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | chr11 | 35197625 | ||||||
| chr11:35197719
|
C | CA | 9 | a0001c0001t0001g0108a0001c0001t0001g0175a0001c0001t0003g0111others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.797-384dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr11 | 35197719 | |||||
| chr11:35198394
|
T | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0032others(18): Show | 21 | HG00323.hp2 HG02027.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.922+148T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198394 | ||||||
| chr11:35198433
|
A | G | 29 | a0001c0002t0001g0219a0001c0002t0001g0306a0001c0002t0002g0014others(26): Show | 29 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.922+187A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198433 | ||||||
| chr11:35198454
|
C | T | 1 | a0001c0001t0006g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.922+208C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198454 | ||||||
| chr11:35198594
|
C | T | 4 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162others(1): Show | 4 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.922+348C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198594 | ||||||
| chr11:35198619
|
T | C | 6 | a0001c0001t0005g0307a0001c0001t0007g0107a0001c0001t0007g0169others(3): Show | 7 | HG02055.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.922+373T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198619 | ||||||
| chr11:35198726
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0240 | 2 | NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.922+480C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198726 | ||||||
| chr11:35198747
|
G | C | 4 | a0001c0008t0002g0347a0001c0008t0005g0362a0001c0008t0005g0363others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.922+501G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198747 | ||||||
| chr11:35198749
|
C | T | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.922+503C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198749 | ||||||
| chr11:35198758
|
G | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(317): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.922+512G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198758 | ||||||
| chr11:35198808
|
C | G | 1 | a0001c0001t0006g0360 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.922+562C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198808 | ||||||
| chr11:35198866
|
C | A | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.922+620C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198866 | ||||||
| chr11:35198916
|
C | T | 36 | a0001c0002t0001g0219a0001c0002t0001g0306a0001c0002t0002g0014others(33): Show | 36 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.922+670C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198916 | ||||||
| chr11:35198924
|
C | T | 45 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(42): Show | 48 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.922+678C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35198924 | ||||||
| chr11:35198967
|
C | CA | 145 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.922+738dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35198967 | |||||
| chr11:35198967
|
C | CAA | 7 | a0001c0001t0001g0135a0001c0001t0001g0159a0001c0001t0001g0203others(4): Show | 7 | HG00438.hp1 NA18969.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.922+737_922+738dup others(2): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35198967 | |||||
| chr11:35198967
|
CA | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0034others(116): Show | 125 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.922+738delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35198967 | |||||
| chr11:35199177
|
C | T | 1 | a0001c0001t0008g0129 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.922+931C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199177 | ||||||
| chr11:35199213
|
A | G | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.922+967A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199213 | ||||||
| chr11:35199283
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.922+1037G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199283 | ||||||
| chr11:35199442
|
G | GA | 39 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(36): Show | 42 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.922+1202dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199442 | |||||
| chr11:35199546
|
G | C | 2 | a0001c0001t0002g0223a0001c0001t0002g0226 | 2 | NA18944.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.922+1300G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199546 | ||||||
| chr11:35199627
|
G | T | 1 | a0001c0001t0020g0365 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.922+1381G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199627 | ||||||
| chr11:35199642
|
AC | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(76): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.922+1397delC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199642 | ||||||
| chr11:35199719
|
A | C | 1 | a0001c0001t0008g0215 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.923-1363A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199719 | ||||||
| chr11:35199793
|
C | T | 1 | a0001c0001t0003g0312 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.923-1289C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199793 | ||||||
| chr11:35199893
|
A | G | 1 | a0001c0001t0028g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.923-1189A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199893 | ||||||
| chr11:35199932
|
T | C | 1 | a0001c0002t0002g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.923-1150T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199932 | ||||||
| chr11:35199934
|
G | GT | 23 | a0001c0001t0002g0063a0002c0003t0001g0112a0002c0003t0001g0244others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.923-1121dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
G | GTT | 11 | a0002c0003t0001g0242a0002c0003t0003g0067a0002c0003t0005g0152others(8): Show | 13 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.923-1122_923-1121d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
GTT | G | 51 | a0001c0001t0002g0261a0001c0001t0005g0307a0001c0001t0006g0006others(48): Show | 54 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(51): Show |
intron_variant | MODIFIER | c.923-1122_923-1121d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
GTTT | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(36): Show | 40 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.923-1123_923-1121d others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
GTTTT | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(77): Show | 83 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.923-1124_923-1121d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
GTTTTT | G | 138 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0048others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.923-1125_923-1121d others(7): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199934
|
GTTTTTT | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0075a0001c0001t0001g0143others(5): Show | 8 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.923-1126_923-1121d others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 35199934 | |||||
| chr11:35199945
|
T | G | 3 | a0001c0001t0005g0170a0001c0001t0005g0173a0001c0001t0021g0091 | 3 | HG02622.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.923-1137T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199945 | ||||||
| chr11:35199967
|
T | G | 20 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0075others(17): Show | 20 | HG00140.hp1 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.923-1115T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35199967 | ||||||
| chr11:35200080
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.923-1002A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200080 | ||||||
| chr11:35200179
|
T | G | 1 | a0002c0003t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.923-903T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200179 | ||||||
| chr11:35200278
|
T | G | 5 | a0001c0002t0006g0106a0001c0007t0002g0099a0001c0007t0002g0301others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-804T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200278 | ||||||
| chr11:35200315
|
T | A | 150 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.923-767T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200315 | ||||||
| chr11:35200330
|
C | G | 1 | a0001c0002t0012g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.923-752C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200330 | ||||||
| chr11:35200358
|
G | A | 14 | a0001c0001t0002g0125a0001c0001t0002g0206a0001c0001t0002g0220others(11): Show | 14 | HG02027.hp1 NA18944.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.923-724G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200358 | ||||||
| chr11:35200363
|
T | C | 45 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(42): Show | 48 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.923-719T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200363 | ||||||
| chr11:35200447
|
G | T | 2 | a0002c0003t0009g0180a0002c0003t0009g0181 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.923-635G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200447 | ||||||
| chr11:35200536
|
T | G | 322 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(319): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.923-546T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200536 | ||||||
| chr11:35200659
|
C | T | 1 | a0001c0001t0018g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.923-423C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200659 | ||||||
| chr11:35200693
|
A | G | 2 | a0001c0002t0002g0253a0001c0007t0005g0185 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.923-389A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200693 | ||||||
| chr11:35200731
|
C | G | 3 | a0001c0002t0002g0253a0001c0002t0003g0199a0001c0007t0005g0185 | 3 | HG02970.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.923-351C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200731 | ||||||
| chr11:35200787
|
T | A | 1 | a0001c0001t0004g0118 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.923-295T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200787 | ||||||
| chr11:35200933
|
C | T | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923-149C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35200933 | ||||||
| chr11:35201018
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.923-64G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 7/17 | chr11 | 35201018 | ||||||
| chr11:35201212
|
A | G | 6 | a0001c0001t0005g0307a0001c0001t0007g0107a0001c0001t0007g0169others(3): Show | 7 | HG02055.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+17A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 8/17 | chr11 | 35201212 | ||||||
| chr11:35201473
|
G | T | 1 | a0001c0001t0020g0344 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1037-198G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 8/17 | chr11 | 35201473 | ||||||
| chr11:35201497
|
T | C | 1 | a0001c0001t0008g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1037-174T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 8/17 | chr11 | 35201497 | ||||||
| chr11:35201611
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(318): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1037-60T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 8/17 | chr11 | 35201611 | ||||||
| chr11:35202106
|
C | T | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1153+319C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202106 | ||||||
| chr11:35202286
|
C | T | 1 | a0001c0001t0007g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1153+499C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202286 | ||||||
| chr11:35202398
|
C | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(317): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1153+611C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202398 | ||||||
| chr11:35202417
|
G | A | 14 | a0001c0002t0001g0219a0001c0002t0002g0014a0001c0002t0002g0184others(11): Show | 14 | HG01099.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+630G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202417 | ||||||
| chr11:35202442
|
C | A | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+655C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202442 | ||||||
| chr11:35202471
|
G | A | 32 | a0001c0001t0001g0145a0001c0001t0001g0208a0001c0001t0001g0209others(29): Show | 32 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1153+684G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202471 | ||||||
| chr11:35202486
|
T | C | 1 | a0001c0001t0006g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1153+699T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202486 | ||||||
| chr11:35202522
|
A | G | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1153+735A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202522 | ||||||
| chr11:35202594
|
C | T | 3 | a0001c0002t0002g0253a0001c0002t0003g0199a0001c0007t0005g0185 | 3 | HG02970.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1153+807C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202594 | ||||||
| chr11:35202597
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1153+810A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202597 | ||||||
| chr11:35202630
|
A | G | 1 | a0002c0005t0008g0248 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1153+843A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202630 | ||||||
| chr11:35202749
|
C | A | 1 | a0001c0002t0012g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1153+962C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202749 | ||||||
| chr11:35202802
|
G | A | 1 | a0001c0001t0013g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1153+1015G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202802 | ||||||
| chr11:35202977
|
A | T | 4 | a0001c0008t0002g0347a0001c0008t0005g0362a0001c0008t0005g0363others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1190A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202977 | ||||||
| chr11:35202984
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(24): Show | 28 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1153+1197G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35202984 | ||||||
| chr11:35203102
|
T | C | 7 | a0001c0001t0005g0307a0001c0001t0007g0107a0001c0001t0007g0169others(4): Show | 8 | HG02055.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153+1315T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203102 | ||||||
| chr11:35203109
|
G | A | 6 | a0001c0001t0006g0197a0001c0001t0013g0013a0004c0009t0002g0186others(3): Show | 6 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153+1322G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203109 | ||||||
| chr11:35203315
|
CT | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(316): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1154-1196delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203315 | ||||||
| chr11:35203439
|
A | G | 5 | a0001c0002t0006g0106a0001c0007t0002g0099a0001c0007t0002g0301others(2): Show | 5 | HG01496.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1073A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203439 | ||||||
| chr11:35203492
|
T | C | 2 | a0001c0002t0002g0253a0001c0007t0005g0185 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1154-1020T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203492 | ||||||
| chr11:35203497
|
T | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0116others(24): Show | 28 | HG00544.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1154-1015T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203497 | ||||||
| chr11:35203708
|
T | TA | 8 | a0001c0001t0002g0063a0001c0001t0002g0082a0002c0003t0009g0179others(5): Show | 8 | HG00733.hp2 HG01358.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154-792dupA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr11 | 35203708 | |||||
| chr11:35203734
|
G | A | 2 | a0001c0001t0003g0074a0001c0001t0036g0326 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1154-778G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35203734 | ||||||
| chr11:35204114
|
T | C | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1154-398T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35204114 | ||||||
| chr11:35204298
|
C | A | 1 | a0001c0001t0022g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1154-214C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35204298 | ||||||
| chr11:35204361
|
C | T | 1 | a0001c0017t0001g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1154-151C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35204361 | ||||||
| chr11:35204427
|
C | A | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-85C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 9/17 | chr11 | 35204427 | ||||||
| chr11:35204650
|
G | A | 2 | a0001c0008t0005g0362a0001c0008t0005g0363 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1282+10G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35204650 | ||||||
| chr11:35204845
|
T | C | 7 | a0001c0001t0005g0307a0001c0001t0007g0107a0001c0001t0007g0169others(4): Show | 8 | HG02055.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282+205T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35204845 | ||||||
| chr11:35204903
|
T | G | 1 | a0001c0001t0008g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1282+263T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35204903 | ||||||
| chr11:35205016
|
A | G | 1 | a0001c0001t0036g0326 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1282+376A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205016 | ||||||
| chr11:35205022
|
T | A | 1 | a0001c0001t0031g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1282+382T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205022 | ||||||
| chr11:35205171
|
C | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0037others(37): Show | 43 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1282+531C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205171 | ||||||
| chr11:35205182
|
T | C | 1 | a0001c0007t0005g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1282+542T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205182 | ||||||
| chr11:35205303
|
G | A | 2 | a0001c0004t0019g0054a0001c0019t0030g0350 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1282+663G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205303 | ||||||
| chr11:35205398
|
C | T | 1 | a0001c0002t0002g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1283-714C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205398 | ||||||
| chr11:35205851
|
T | A | 1 | a0001c0001t0028g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1283-261T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 10/17 | chr11 | 35205851 | ||||||
| chr11:35206250
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG01074.hp1 | splice_region_variant&intron_variant | LOW | c.1414+7G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206250 | ||||||
| chr11:35206523
|
G | C | 1 | a0001c0001t0028g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1414+280G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206523 | ||||||
| chr11:35206666
|
T | TG | 10 | a0001c0001t0001g0175a0001c0001t0002g0063a0001c0001t0004g0109others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1414+425dupG | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206666 | |||||
| chr11:35206666
|
T | TGG | 4 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0001t0002g0266others(1): Show | 4 | HG01169.hp1 HG01261.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+424_1414+425d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206666 | |||||
| chr11:35206666
|
T | TGGA | 102 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(99): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1414+425_1414+426i others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206666 | |||||
| chr11:35206666
|
T | TGGAG | 22 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0089others(19): Show | 22 | HG00621.hp1 HG00738.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1414+425_1414+426i others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206666 | |||||
| chr11:35206667
|
G | GGA | 60 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0037others(57): Show | 62 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1414+425_1414+426i others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206667 | |||||
| chr11:35206668
|
G | GA | 65 | a0001c0001t0001g0048a0001c0001t0001g0190a0001c0001t0001g0209others(62): Show | 68 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1414+425_1414+426i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206668 | ||||||
| chr11:35206668
|
G | GAGC | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+425_1414+426i others(5): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206668 | ||||||
| chr11:35206668
|
GT | G | 3 | a0001c0001t0006g0360a0001c0001t0028g0251a0001c0004t0019g0054 | 3 | HG01884.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1414+426delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206668 | ||||||
| chr11:35206669
|
T | A | 45 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0115others(42): Show | 47 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1414+426T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206669 | ||||||
| chr11:35206669
|
T | C | 13 | a0001c0001t0006g0166a0001c0001t0006g0168a0001c0001t0006g0176others(10): Show | 14 | HG02451.hp2 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1414+426T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206669 | ||||||
| chr11:35206669
|
T | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(253): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1414+426T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206669 | ||||||
| chr11:35206670
|
G | GGC | 20 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0158others(17): Show | 21 | HG00408.hp1 HG00597.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1414+428_1414+429i others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 35206670 | |||||
| chr11:35206671
|
G | GCA | 18 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG00673.hp1 HG02027.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.1414+428_1414+429i others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206671 | ||||||
| chr11:35206741
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1414+498A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206741 | ||||||
| chr11:35206747
|
C | CT | 315 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(312): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1414+504_1414+505i others(3): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206747 | ||||||
| chr11:35206769
|
C | T | 1 | a0001c0004t0001g0277 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1414+526C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206769 | ||||||
| chr11:35206899
|
C | G | 9 | a0001c0001t0005g0307a0001c0001t0007g0095a0001c0001t0007g0096others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1414+656C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35206899 | ||||||
| chr11:35207309
|
A | G | 1 | a0001c0001t0004g0027 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1415-796A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207309 | ||||||
| chr11:35207373
|
G | A | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1415-732G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207373 | ||||||
| chr11:35207548
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1415-557A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207548 | ||||||
| chr11:35207706
|
G | A | 1 | a0005c0012t0003g0011 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1415-399G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207706 | ||||||
| chr11:35207724
|
A | G | 8 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(5): Show | 9 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1415-381A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207724 | ||||||
| chr11:35207829
|
T | C | 1 | a0001c0001t0006g0227 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1415-276T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 11/17 | chr11 | 35207829 | ||||||
| chr11:35208292
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1516+86G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35208292 | ||||||
| chr11:35208309
|
T | C | 16 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(13): Show | 17 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1516+103T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35208309 | ||||||
| chr11:35208511
|
T | G | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1516+305T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35208511 | ||||||
| chr11:35208991
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0254a0001c0001t0001g0292others(4): Show | 7 | HG01071.hp2 HG01256.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516+785G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35208991 | ||||||
| chr11:35209058
|
G | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(282): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1516+852G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209058 | ||||||
| chr11:35209193
|
C | CAG | 21 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(18): Show | 22 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.1517-771_1517-770d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr11 | 35209193 | |||||
| chr11:35209321
|
A | G | 3 | a0001c0001t0002g0261a0001c0004t0007g0364a0002c0003t0009g0218 | 3 | HG02258.hp2 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1517-644A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209321 | ||||||
| chr11:35209325
|
G | A | 8 | a0001c0001t0002g0085a0001c0001t0002g0125a0001c0001t0002g0206others(5): Show | 8 | HG00673.hp1 HG02027.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-640G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209325 | ||||||
| chr11:35209372
|
G | A | 21 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(18): Show | 22 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.1517-593G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209372 | ||||||
| chr11:35209421
|
T | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517-544T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209421 | ||||||
| chr11:35209475
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1517-490G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209475 | ||||||
| chr11:35209546
|
C | T | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1517-419C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209546 | ||||||
| chr11:35209596
|
G | A | 16 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(13): Show | 17 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1517-369G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209596 | ||||||
| chr11:35209651
|
T | C | 1 | a0001c0001t0008g0215 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1517-314T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209651 | ||||||
| chr11:35209686
|
G | A | 1 | a0003c0006t0003g0346 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1517-279G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209686 | ||||||
| chr11:35209836
|
G | A | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1517-129G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 12/17 | chr11 | 35209836 | ||||||
| chr11:35210080
|
T | C | 16 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(13): Show | 17 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1606+26T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210080 | ||||||
| chr11:35210156
|
G | A | 1 | a0001c0014t0003g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1606+102G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210156 | ||||||
| chr11:35210230
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1606+176G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210230 | ||||||
| chr11:35210250
|
AT | A | 5 | a0001c0001t0008g0299a0001c0001t0009g0105a0001c0001t0028g0251others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1606+199delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 35210250 | |||||
| chr11:35210280
|
C | T | 2 | a0002c0003t0009g0180a0002c0003t0009g0181 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1606+226C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210280 | ||||||
| chr11:35210531
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1606+477T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210531 | ||||||
| chr11:35210673
|
C | T | 13 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(10): Show | 14 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1607-573C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210673 | ||||||
| chr11:35210674
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1607-572G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210674 | ||||||
| chr11:35210700
|
A | G | 3 | a0001c0002t0002g0253a0001c0002t0005g0101a0001c0002t0012g0178 | 3 | HG02109.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1607-546A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210700 | ||||||
| chr11:35210750
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1607-496G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 13/17 | chr11 | 35210750 | ||||||
| chr11:35211674
|
A | ATG | 4 | a0001c0001t0001g0150a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG01433.hp2 NA18940.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810+255_1810+256d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35211674 | |||||
| chr11:35211674
|
A | G | 3 | a0002c0003t0009g0179a0002c0003t0009g0180a0002c0003t0009g0181 | 3 | HG01891.hp2 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1810+225A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35211674 | ||||||
| chr11:35211674
|
ATG | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(220): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1810+255_1810+256d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35211674 | |||||
| chr11:35211674
|
ATGTG | A | 67 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0211others(64): Show | 71 | HG00140.hp2 HG00609.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.1810+253_1810+256d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35211674 | |||||
| chr11:35211674
|
ATGTGTG | A | 13 | a0001c0002t0003g0199a0001c0002t0006g0106a0001c0002t0008g0102others(10): Show | 13 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1810+251_1810+256d others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35211674 | |||||
| chr11:35211674
|
ATGTGTGT others(1): Show |
A | 22 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(19): Show | 23 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.1810+249_1810+256d others(10): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35211674 | |||||
| chr11:35211800
|
G | A | 5 | a0001c0002t0003g0199a0001c0010t0007g0133a0001c0010t0007g0161others(2): Show | 5 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810+351G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35211800 | ||||||
| chr11:35211927
|
G | A | 5 | a0001c0002t0003g0199a0001c0010t0007g0133a0001c0010t0007g0161others(2): Show | 5 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810+478G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35211927 | ||||||
| chr11:35212037
|
C | A | 1 | a0001c0004t0004g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1810+588C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212037 | ||||||
| chr11:35212068
|
A | C | 16 | a0001c0001t0002g0250a0001c0001t0006g0006a0001c0001t0006g0166others(13): Show | 17 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1810+619A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212068 | ||||||
| chr11:35212231
|
A | T | 26 | a0001c0001t0001g0034a0001c0001t0001g0236a0001c0001t0003g0083others(23): Show | 27 | HG00140.hp2 HG00609.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1810+782A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212231 | ||||||
| chr11:35212309
|
T | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1810+860T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212309 | ||||||
| chr11:35212402
|
A | AT | 19 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(16): Show | 19 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1810+964dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35212402 | |||||
| chr11:35212402
|
AT | A | 13 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(10): Show | 14 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1810+964delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35212402 | |||||
| chr11:35212550
|
G | A | 1 | a0004c0009t0002g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1810+1101G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212550 | ||||||
| chr11:35212679
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1810+1230G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212679 | ||||||
| chr11:35212886
|
C | T | 4 | a0002c0003t0009g0179a0002c0003t0009g0180a0002c0003t0009g0181others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810+1437C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212886 | ||||||
| chr11:35212917
|
G | A | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810+1468G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35212917 | ||||||
| chr11:35213122
|
C | A | 11 | a0001c0001t0005g0307a0001c0001t0006g0360a0001c0001t0007g0095others(8): Show | 12 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1810+1673C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213122 | ||||||
| chr11:35213135
|
G | T | 3 | a0001c0001t0002g0250a0001c0001t0007g0094a0001c0001t0008g0252 | 3 | HG02723.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1810+1686G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213135 | ||||||
| chr11:35213251
|
A | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0226 | 2 | NA18944.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1811-1601A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213251 | ||||||
| chr11:35213479
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1811-1373C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213479 | ||||||
| chr11:35213506
|
G | A | 1 | a0005c0013t0003g0352 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1811-1346G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213506 | ||||||
| chr11:35213601
|
G | A | 5 | a0001c0001t0006g0360a0004c0009t0002g0186a0004c0009t0002g0300others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1811-1251G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213601 | ||||||
| chr11:35213638
|
C | T | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-1214C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213638 | ||||||
| chr11:35213654
|
A | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1811-1198A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213654 | ||||||
| chr11:35213689
|
G | A | 1 | a0002c0003t0009g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1811-1163G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213689 | ||||||
| chr11:35213698
|
G | GTGGAGAT others(5): Show |
5 | a0001c0002t0003g0199a0001c0010t0007g0133a0001c0010t0007g0161others(2): Show | 5 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1811-1151_1811-115 others(16): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35213698 | |||||
| chr11:35213765
|
AGTGGGAG others(7): Show |
A | 21 | a0001c0001t0001g0034a0001c0001t0001g0236a0001c0001t0003g0083others(18): Show | 22 | HG00140.hp2 HG00609.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1811-1082_1811-106 others(18): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35213765 | |||||
| chr11:35213775
|
T | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1811-1077T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213775 | ||||||
| chr11:35213852
|
A | C | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-1000A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213852 | ||||||
| chr11:35213883
|
G | A | 4 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162others(1): Show | 4 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-969G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35213883 | ||||||
| chr11:35213997
|
TA | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(123): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1811-842delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr11 | 35213997 | |||||
| chr11:35214094
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1811-758T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214094 | ||||||
| chr11:35214373
|
A | G | 2 | a0001c0001t0003g0016a0001c0001t0003g0357 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1811-479A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214373 | ||||||
| chr11:35214383
|
C | T | 4 | a0004c0009t0002g0186a0004c0009t0002g0300a0004c0009t0017g0092others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1811-469C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214383 | ||||||
| chr11:35214558
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1811-294G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214558 | ||||||
| chr11:35214578
|
T | C | 26 | a0001c0001t0001g0034a0001c0001t0001g0236a0001c0001t0003g0083others(23): Show | 27 | HG00140.hp2 HG00609.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1811-274T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214578 | ||||||
| chr11:35214684
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1811-168G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214684 | ||||||
| chr11:35214839
|
T | C | 3 | a0001c0001t0002g0261a0001c0004t0007g0364a0002c0003t0009g0218 | 3 | HG02258.hp2 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1811-13T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 14/17 | chr11 | 35214839 | ||||||
| chr11:35215007
|
T | C | 2 | a0001c0001t0006g0176a0001c0001t0006g0177 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1873+93T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215007 | ||||||
| chr11:35215032
|
A | G | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1873+118A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215032 | ||||||
| chr11:35215051
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1873+137C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215051 | ||||||
| chr11:35215104
|
C | A | 1 | a0001c0001t0005g0307 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1873+190C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215104 | ||||||
| chr11:35215187
|
G | A | 25 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0250others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1873+273G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215187 | ||||||
| chr11:35215231
|
G | T | 5 | a0001c0001t0008g0299a0001c0001t0009g0105a0001c0001t0028g0251others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1873+317G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215231 | ||||||
| chr11:35215257
|
C | A | 335 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(332): Show | 346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.1873+343C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215257 | ||||||
| chr11:35215376
|
C | A | 5 | a0001c0002t0003g0199a0001c0010t0007g0133a0001c0010t0007g0161others(2): Show | 5 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1873+462C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215376 | ||||||
| chr11:35215496
|
G | T | 1 | a0001c0001t0001g0287 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1873+582G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215496 | ||||||
| chr11:35215509
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0108 | 2 | NA19060.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1873+595T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215509 | ||||||
| chr11:35215698
|
C | A | 1 | a0001c0001t0004g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1873+784C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215698 | ||||||
| chr11:35215729
|
G | A | 35 | a0001c0001t0001g0065a0001c0001t0001g0209a0001c0001t0001g0210others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1873+815G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215729 | ||||||
| chr11:35215865
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(107): Show | 113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1873+951C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215865 | ||||||
| chr11:35215880
|
C | A | 1 | a0001c0001t0006g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1873+966C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35215880 | ||||||
| chr11:35216318
|
C | T | 1 | a0001c0001t0013g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1873+1404C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216318 | ||||||
| chr11:35216477
|
C | T | 52 | a0001c0001t0001g0158a0001c0001t0002g0010a0001c0001t0002g0032others(49): Show | 55 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1873+1563C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216477 | ||||||
| chr11:35216575
|
T | C | 4 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162others(1): Show | 4 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+1661T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216575 | ||||||
| chr11:35216753
|
A | T | 1 | a0001c0001t0006g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1873+1839A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216753 | ||||||
| chr11:35216906
|
A | G | 1 | a0001c0001t0004g0026 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1873+1992A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216906 | ||||||
| chr11:35216912
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(315): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1873+1998A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35216912 | ||||||
| chr11:35217031
|
T | C | 25 | a0001c0001t0001g0034a0001c0001t0001g0236a0001c0001t0003g0083others(22): Show | 26 | HG00140.hp2 HG00609.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1873+2117T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217031 | ||||||
| chr11:35217115
|
TC | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1874-2199delC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr11 | 35217115 | |||||
| chr11:35217267
|
C | CT | 103 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0175others(100): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1874-2034dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr11 | 35217267 | |||||
| chr11:35217267
|
CT | C | 11 | a0001c0001t0001g0202a0001c0001t0002g0250a0001c0001t0002g0348others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1874-2034delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr11 | 35217267 | |||||
| chr11:35217356
|
GA | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(16): Show | 19 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1874-1946delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr11 | 35217356 | |||||
| chr11:35217473
|
C | T | 3 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162 | 3 | HG01256.hp1 HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1874-1843C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217473 | ||||||
| chr11:35217542
|
G | A | 1 | a0001c0001t0006g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1874-1774G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217542 | ||||||
| chr11:35217598
|
G | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1874-1718G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217598 | ||||||
| chr11:35217657
|
T | C | 2 | a0001c0001t0003g0016a0001c0001t0003g0357 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1874-1659T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217657 | ||||||
| chr11:35217760
|
A | G | 1 | a0002c0003t0009g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1874-1556A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217760 | ||||||
| chr11:35217793
|
T | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1874-1523T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217793 | ||||||
| chr11:35217988
|
A | G | 23 | a0001c0001t0001g0034a0001c0001t0001g0236a0001c0001t0003g0083others(20): Show | 24 | HG00140.hp2 HG00609.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1874-1328A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35217988 | ||||||
| chr11:35218015
|
T | G | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1874-1301T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218015 | ||||||
| chr11:35218018
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(315): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1874-1298A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218018 | ||||||
| chr11:35218115
|
T | C | 2 | a0001c0002t0008g0102a0001c0002t0008g0171 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1874-1201T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218115 | ||||||
| chr11:35218154
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1874-1162G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218154 | ||||||
| chr11:35218174
|
C | T | 3 | a0001c0001t0012g0005a0001c0002t0002g0297a0001c0002t0012g0165 | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1874-1142C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218174 | ||||||
| chr11:35218236
|
T | C | 11 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(8): Show | 12 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1874-1080T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218236 | ||||||
| chr11:35218341
|
T | G | 1 | a0001c0001t0002g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1874-975T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218341 | ||||||
| chr11:35218360
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(120): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1874-956C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218360 | ||||||
| chr11:35218488
|
C | T | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1874-828C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218488 | ||||||
| chr11:35218529
|
A | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1874-787A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218529 | ||||||
| chr11:35218549
|
AAT | A | 52 | a0001c0001t0001g0158a0001c0001t0002g0010a0001c0001t0002g0032others(49): Show | 55 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1874-766_1874-765d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218549 | ||||||
| chr11:35218569
|
C | T | 1 | a0001c0001t0023g0021 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1874-747C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218569 | ||||||
| chr11:35218697
|
G | A | 2 | a0001c0001t0002g0250a0001c0001t0008g0252 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1874-619G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218697 | ||||||
| chr11:35218782
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1874-534A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218782 | ||||||
| chr11:35218886
|
G | A | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1874-430G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35218886 | ||||||
| chr11:35219053
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1874-263C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35219053 | ||||||
| chr11:35219153
|
G | A | 1 | a0001c0004t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1874-163G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35219153 | ||||||
| chr11:35219177
|
T | C | 3 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162 | 3 | HG01256.hp1 HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1874-139T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35219177 | ||||||
| chr11:35219242
|
T | A | 52 | a0001c0001t0001g0158a0001c0001t0002g0010a0001c0001t0002g0032others(49): Show | 55 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1874-74T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 15/17 | chr11 | 35219242 | ||||||
| chr11:35219556
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1945+169T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219556 | ||||||
| chr11:35219600
|
A | C | 2 | a0001c0001t0002g0250a0001c0001t0008g0252 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1945+213A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219600 | ||||||
| chr11:35219682
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(159): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1945+295T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219682 | ||||||
| chr11:35219737
|
A | C | 1 | a0001c0001t0002g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1945+350A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219737 | ||||||
| chr11:35219788
|
C | T | 5 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG00741.hp1 HG01081.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+401C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219788 | ||||||
| chr11:35219817
|
G | A | 2 | a0001c0002t0005g0101a0001c0002t0012g0178 | 2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1945+430G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219817 | ||||||
| chr11:35219830
|
A | C | 1 | a0001c0001t0013g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1945+443A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219830 | ||||||
| chr11:35219864
|
AT | A | 40 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0108others(37): Show | 41 | HG00140.hp2 HG00609.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1945+486delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr11 | 35219864 | |||||
| chr11:35219938
|
G | A | 52 | a0001c0001t0001g0158a0001c0001t0002g0010a0001c0001t0002g0032others(49): Show | 55 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1945+551G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35219938 | ||||||
| chr11:35220090
|
C | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(130): Show | 137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1945+703C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220090 | ||||||
| chr11:35220129
|
G | C | 5 | a0001c0001t0008g0295a0001c0001t0022g0090a0001c0002t0008g0102others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+742G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220129 | ||||||
| chr11:35220163
|
A | C | 11 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(8): Show | 12 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1945+776A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220163 | ||||||
| chr11:35220183
|
A | C | 2 | a0001c0008t0002g0347a0001c0008t0014g0172 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1945+796A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220183 | ||||||
| chr11:35220367
|
G | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(266): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1945+980G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220367 | ||||||
| chr11:35220373
|
CT | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(22): Show | 25 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1945+987delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220373 | ||||||
| chr11:35220374
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(231): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1945+987T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220374 | ||||||
| chr11:35220442
|
T | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(217): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1945+1055T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220442 | ||||||
| chr11:35220738
|
C | A | 5 | a0001c0010t0007g0133a0001c0010t0007g0161a0001c0010t0007g0162others(2): Show | 5 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946-916C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220738 | ||||||
| chr11:35220763
|
CT | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0022others(210): Show | 222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1946-870delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr11 | 35220763 | |||||
| chr11:35220763
|
CTT | C | 30 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0288others(27): Show | 30 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1946-871_1946-870d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr11 | 35220763 | |||||
| chr11:35220828
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(123): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1946-826G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220828 | ||||||
| chr11:35220876
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(211): Show | 222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1946-778C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220876 | ||||||
| chr11:35220915
|
C | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(25): Show | 29 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1946-739C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220915 | ||||||
| chr11:35220953
|
G | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(211): Show | 222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1946-701G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220953 | ||||||
| chr11:35220988
|
T | G | 3 | a0001c0002t0002g0253a0001c0002t0005g0101a0001c0002t0012g0178 | 3 | HG02109.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1946-666T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220988 | ||||||
| chr11:35220995
|
G | A | 6 | a0001c0002t0003g0199a0001c0010t0007g0133a0001c0010t0007g0161others(3): Show | 6 | HG01099.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1946-659G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35220995 | ||||||
| chr11:35221043
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1946-611G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221043 | ||||||
| chr11:35221065
|
G | A | 1 | a0001c0002t0002g0196 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1946-589G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221065 | ||||||
| chr11:35221106
|
C | T | 26 | a0001c0001t0001g0065a0001c0001t0003g0016a0001c0001t0003g0023others(23): Show | 26 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1946-548C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221106 | ||||||
| chr11:35221113
|
C | T | 308 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(305): Show | 318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1946-541C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221113 | ||||||
| chr11:35221305
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1946-349C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221305 | ||||||
| chr11:35221360
|
G | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(211): Show | 222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1946-294G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221360 | ||||||
| chr11:35221379
|
A | AGTCATCC others(3967): Show |
1 | a0001c0001t0005g0028 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1946-257_1946-256i others(3976): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr11 | 35221379 | |||||
| chr11:35221436
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1946-218C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221436 | ||||||
| chr11:35221513
|
A | G | 1 | a0001c0001t0006g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1946-141A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221513 | ||||||
| chr11:35221619
|
A | T | 2 | a0001c0001t0013g0013a0001c0002t0038g0103 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1946-35A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 16/17 | chr11 | 35221619 | ||||||
| chr11:35221886
|
C | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0002g0266others(25): Show | 29 | HG00639.hp2 HG00733.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.2024+154C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35221886 | ||||||
| chr11:35221887
|
C | G | 26 | a0001c0001t0001g0065a0001c0001t0003g0016a0001c0001t0003g0023others(23): Show | 26 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2024+155C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35221887 | ||||||
| chr11:35221902
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2024+170C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35221902 | ||||||
| chr11:35221968
|
G | A | 1 | a0001c0017t0001g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2024+236G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35221968 | ||||||
| chr11:35222001
|
T | C | 1 | a0002c0005t0009g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2024+269T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222001 | ||||||
| chr11:35222193
|
G | T | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2024+461G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222193 | ||||||
| chr11:35222258
|
A | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0204a0001c0001t0001g0345 | 3 | NA18965.hp2 NA18999.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2024+526A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222258 | ||||||
| chr11:35222266
|
G | GTATTGGC others(29): Show |
8 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0050others(5): Show | 9 | HG00597.hp1 NA18948.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.2024+559_2024+594d others(38): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35222266 | |||||
| chr11:35222292
|
G | A | 1 | a0001c0002t0001g0306 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2024+560G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222292 | ||||||
| chr11:35222292
|
G | C | 1 | a0001c0002t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2024+560G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222292 | ||||||
| chr11:35222436
|
A | G | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2024+704A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222436 | ||||||
| chr11:35222497
|
G | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(310): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.2024+765G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222497 | ||||||
| chr11:35222511
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(213): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.2024+779A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222511 | ||||||
| chr11:35222598
|
A | AAT | 45 | a0001c0001t0001g0065a0001c0001t0002g0032a0001c0001t0003g0016others(42): Show | 45 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2024+884_2024+885d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35222598 | |||||
| chr11:35222598
|
A | AATAT | 13 | a0001c0001t0001g0034a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 14 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2024+882_2024+885d others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35222598 | |||||
| chr11:35222598
|
A | T | 2 | a0001c0002t0007g0012a0001c0002t0007g0305 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2024+866A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222598 | ||||||
| chr11:35222598
|
AAT | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0144others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.2024+884_2024+885d others(4): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35222598 | |||||
| chr11:35222599
|
A | T | 1 | a0001c0002t0006g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2024+867A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222599 | ||||||
| chr11:35222600
|
T | A | 1 | a0001c0002t0006g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2024+868T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222600 | ||||||
| chr11:35222616
|
T | C | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0157others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2024+884T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222616 | ||||||
| chr11:35222678
|
GGTATAAA others(15): Show |
G | 1 | a0001c0001t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2024+963_2024+984d others(24): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35222678 | |||||
| chr11:35222787
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2024+1055G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222787 | ||||||
| chr11:35222877
|
G | A | 1 | a0001c0002t0006g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2024+1145G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222877 | ||||||
| chr11:35222910
|
C | T | 2 | a0003c0006t0003g0123a0003c0006t0003g0329 | 2 | HG01515.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.2024+1178C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35222910 | ||||||
| chr11:35223027
|
C | T | 103 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0022others(100): Show | 104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2024+1295C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223027 | ||||||
| chr11:35223096
|
C | A | 29 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0035others(26): Show | 30 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2024+1364C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223096 | ||||||
| chr11:35223122
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2024+1390A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223122 | ||||||
| chr11:35223198
|
A | AT | 17 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(14): Show | 19 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.2024+1474dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35223198 | |||||
| chr11:35223297
|
T | C | 1 | a0001c0001t0016g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2024+1565T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223297 | ||||||
| chr11:35223340
|
T | C | 62 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(59): Show | 63 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2024+1608T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223340 | ||||||
| chr11:35223385
|
TC | T | 10 | a0001c0001t0006g0360a0001c0001t0021g0091a0001c0001t0022g0090others(7): Show | 10 | HG01099.hp2 HG01109.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2024+1655delC | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35223385 | |||||
| chr11:35223459
|
G | A | 2 | a0001c0002t0005g0359a0001c0007t0005g0185 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2024+1727G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223459 | ||||||
| chr11:35223580
|
C | G | 1 | a0001c0002t0012g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2024+1848C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223580 | ||||||
| chr11:35223618
|
A | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 11 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.2024+1886A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223618 | ||||||
| chr11:35223740
|
G | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0338a0001c0001t0002g0010others(200): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.2024+2008G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223740 | ||||||
| chr11:35223900
|
G | A | 62 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(59): Show | 63 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2024+2168G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35223900 | ||||||
| chr11:35224000
|
G | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(9): Show | 13 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2024+2268G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224000 | ||||||
| chr11:35224145
|
T | C | 1 | a0001c0002t0005g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2024+2413T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224145 | ||||||
| chr11:35224236
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0022others(50): Show | 54 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2024+2504G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224236 | ||||||
| chr11:35224360
|
T | C | 75 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(72): Show | 77 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.2024+2628T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224360 | ||||||
| chr11:35224363
|
C | A | 1 | a0001c0001t0022g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2024+2631C>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224363 | ||||||
| chr11:35224432
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0338a0001c0001t0002g0033others(19): Show | 26 | HG00735.hp2 HG01074.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.2024+2700T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224432 | ||||||
| chr11:35224495
|
T | C | 3 | a0001c0001t0012g0005a0001c0002t0012g0165a0001c0002t0012g0178 | 4 | HG02280.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2024+2763T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224495 | ||||||
| chr11:35224523
|
G | T | 23 | a0001c0001t0004g0027a0001c0001t0004g0323a0001c0001t0005g0028others(20): Show | 23 | HG02071.hp2 HG02132.hp2 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.2024+2791G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35224523 | ||||||
| chr11:35225126
|
A | AAGCACTT others(40): Show |
29 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0035others(26): Show | 30 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2024+3395_2024+339 others(51): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35225126 | |||||
| chr11:35225261
|
G | T | 1 | a0001c0001t0008g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2024+3529G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225261 | ||||||
| chr11:35225298
|
G | C | 24 | a0001c0001t0004g0027a0001c0001t0004g0131a0001c0001t0004g0323others(21): Show | 24 | HG02071.hp2 HG02132.hp2 HG02622.hp2 others(21): Show |
intron_variant | MODIFIER | c.2024+3566G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225298 | ||||||
| chr11:35225316
|
T | C | 29 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0035others(26): Show | 30 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2024+3584T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225316 | ||||||
| chr11:35225318
|
A | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(323): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.2024+3586A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225318 | ||||||
| chr11:35225436
|
G | A | 1 | a0001c0019t0030g0350 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2025-3693G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225436 | ||||||
| chr11:35225597
|
A | C | 1 | a0002c0005t0010g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2025-3532A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225597 | ||||||
| chr11:35225601
|
G | T | 1 | a0002c0005t0010g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2025-3528G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225601 | ||||||
| chr11:35225606
|
C | T | 1 | a0002c0005t0010g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2025-3523C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225606 | ||||||
| chr11:35225624
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2025-3505G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225624 | ||||||
| chr11:35225712
|
G | T | 15 | a0001c0001t0002g0250a0001c0001t0008g0215a0001c0001t0008g0252others(12): Show | 15 | HG00408.hp2 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2025-3417G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225712 | ||||||
| chr11:35225826
|
AAAAC | A | 4 | a0001c0001t0021g0091a0001c0007t0011g0087a0001c0007t0011g0088others(1): Show | 4 | HG01099.hp2 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2025-3279_2025-327 others(8): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35225826 | |||||
| chr11:35225908
|
A | G | 9 | a0001c0001t0008g0215a0001c0001t0008g0252a0001c0001t0008g0299others(6): Show | 9 | HG00408.hp2 HG01243.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2025-3221A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225908 | ||||||
| chr11:35225950
|
A | G | 1 | a0001c0001t0006g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2025-3179A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35225950 | ||||||
| chr11:35226069
|
C | T | 26 | a0001c0001t0004g0027a0001c0001t0004g0131a0001c0001t0004g0323others(23): Show | 26 | HG02071.hp1 HG02071.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.2025-3060C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226069 | ||||||
| chr11:35226070
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(9): Show | 13 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025-3059G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226070 | ||||||
| chr11:35226123
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2025-3006C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226123 | ||||||
| chr11:35226335
|
A | C | 4 | a0001c0001t0013g0013a0001c0001t0013g0097a0001c0002t0038g0103others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2025-2794A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226335 | ||||||
| chr11:35226380
|
T | C | 2 | a0001c0001t0001g0205a0001c0001t0002g0020 | 2 | NA18946.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2025-2749T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226380 | ||||||
| chr11:35226381
|
A | G | 12 | a0001c0001t0009g0105a0001c0002t0002g0184a0001c0002t0009g0182others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2025-2748A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226381 | ||||||
| chr11:35226512
|
A | G | 30 | a0001c0001t0002g0063a0001c0001t0009g0105a0001c0001t0010g0072others(27): Show | 30 | HG00099.hp2 HG00733.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2025-2617A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226512 | ||||||
| chr11:35226628
|
C | T | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2025-2501C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226628 | ||||||
| chr11:35226647
|
CA | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(9): Show | 13 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025-2480delA | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226647 | |||||
| chr11:35226764
|
C | G | 4 | a0001c0001t0013g0013a0001c0001t0013g0097a0001c0002t0038g0103others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2025-2365C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226764 | ||||||
| chr11:35226819
|
T | A | 1 | a0001c0001t0002g0285 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2025-2310T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226819 | ||||||
| chr11:35226868
|
CT | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(9): Show | 13 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025-2258delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226868 | |||||
| chr11:35226880
|
C | CT | 39 | a0001c0001t0001g0147a0001c0001t0001g0240a0001c0001t0001g0309others(36): Show | 40 | HG00408.hp2 HG01099.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.2025-2227dupT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226880 | |||||
| chr11:35226880
|
C | CTT | 14 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(11): Show | 15 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2025-2228_2025-222 others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226880 | |||||
| chr11:35226880
|
CT | C | 30 | a0001c0001t0001g0130a0001c0001t0001g0317a0001c0001t0002g0063others(27): Show | 30 | HG00323.hp1 HG00609.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.2025-2227delT | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226880 | |||||
| chr11:35226880
|
CTT | C | 6 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0010g0232others(3): Show | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2025-2228_2025-222 others(6): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr11 | 35226880 | |||||
| chr11:35226900
|
TTTGAGAC others(1): Show |
T | 18 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(15): Show | 18 | HG02071.hp2 HG02132.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2025-2228_2025-222 others(12): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226900 | ||||||
| chr11:35226901
|
TTGAGACG | T | 36 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(33): Show | 37 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2025-2227_2025-222 others(11): Show |
CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226901 | ||||||
| chr11:35226908
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2025-2221G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226908 | ||||||
| chr11:35226912
|
T | A | 54 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(51): Show | 55 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.2025-2217T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226912 | ||||||
| chr11:35226915
|
T | C | 2 | a0001c0001t0006g0197a0001c0001t0008g0295 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2025-2214T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226915 | ||||||
| chr11:35226937
|
T | A | 1 | a0002c0005t0002g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2025-2192T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226937 | ||||||
| chr11:35226937
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2025-2192T>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226937 | ||||||
| chr11:35226940
|
G | A | 1 | a0001c0001t0005g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2025-2189G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226940 | ||||||
| chr11:35226944
|
A | G | 55 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(52): Show | 56 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2025-2185A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226944 | ||||||
| chr11:35226979
|
G | C | 7 | a0001c0001t0002g0085a0001c0001t0002g0125a0001c0001t0002g0206others(4): Show | 7 | HG02027.hp1 NA18944.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.2025-2150G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35226979 | ||||||
| chr11:35227051
|
C | T | 1 | a0001c0010t0033g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2025-2078C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227051 | ||||||
| chr11:35227116
|
C | G | 34 | a0001c0001t0004g0004a0001c0001t0004g0026a0001c0001t0004g0027others(31): Show | 35 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.2025-2013C>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227116 | ||||||
| chr11:35227182
|
G | C | 1 | a0001c0001t0006g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2025-1947G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227182 | ||||||
| chr11:35227233
|
T | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0338others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2025-1896T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227233 | ||||||
| chr11:35227566
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2025-1563A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227566 | ||||||
| chr11:35227703
|
C | T | 1 | a0001c0001t0021g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2025-1426C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227703 | ||||||
| chr11:35227868
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2025-1261G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227868 | ||||||
| chr11:35227884
|
T | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0166a0001c0001t0006g0168others(9): Show | 13 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025-1245T>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227884 | ||||||
| chr11:35227887
|
C | T | 30 | a0001c0001t0002g0063a0001c0001t0009g0105a0001c0001t0010g0072others(27): Show | 30 | HG00099.hp2 HG00733.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2025-1242C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227887 | ||||||
| chr11:35227951
|
A | G | 1 | a0002c0003t0010g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2025-1178A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35227951 | ||||||
| chr11:35228123
|
A | G | 181 | a0001c0001t0002g0010a0001c0001t0002g0020a0001c0001t0002g0032others(178): Show | 188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2025-1006A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228123 | ||||||
| chr11:35228145
|
T | G | 1 | a0001c0001t0022g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2025-984T>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228145 | ||||||
| chr11:35228203
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0121a0001c0001t0001g0175others(1): Show | 4 | HG01928.hp1 NA18944.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.2025-926G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228203 | ||||||
| chr11:35228271
|
G | A | 33 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0158others(30): Show | 34 | HG00673.hp2 HG01109.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2025-858G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228271 | ||||||
| chr11:35228460
|
G | T | 2 | a0001c0010t0007g0161a0001c0010t0007g0162 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2025-669G>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228460 | ||||||
| chr11:35228466
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2025-663A>G | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228466 | ||||||
| chr11:35228549
|
A | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0151 | 2 | NA19006.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2025-580A>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228549 | ||||||
| chr11:35228560
|
G | A | 10 | a0001c0001t0008g0129a0001c0001t0008g0215a0001c0001t0008g0252others(7): Show | 10 | HG00408.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2025-569G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228560 | ||||||
| chr11:35228608
|
G | C | 1 | a0001c0001t0002g0256 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2025-521G>C | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228608 | ||||||
| chr11:35228719
|
C | T | 5 | a0001c0001t0010g0072a0001c0001t0010g0073a0002c0003t0010g0015others(2): Show | 5 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2025-410C>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228719 | ||||||
| chr11:35228759
|
G | A | 1 | a0001c0002t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2025-370G>A | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228759 | ||||||
| chr11:35228971
|
A | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(116): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2025-158A>T | CD44 | ENSG00000026508.21 | transcript | ENST00000428726.8 | protein_coding | 17/17 | chr11 | 35228971 |