Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6768 |
|---|---|
| ensemblid | ENSG00000149418.11 |
| hgncid | 11344 |
| symbol | ST14 |
| name | ST14 transmembrane serine protease matriptase |
| refseq_nuc | NM_021978.4 |
| refseq_prot | NP_068813.1 |
| ensembl_nuc | ENST00000278742.6 |
| ensembl_prot | ENSP00000278742.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 130159782 |
| end | 130210362 |
| strand | + |
| ver | v1.2 |
| region | chr11:130159782-130210362 |
| region5000 | chr11:130154782-130215362 |
| regionname0 | ST14_chr11_130159782_130210362 |
| regionname5000 | ST14_chr11_130154782_130215362 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 855 | 221 | 43 | 42 | 98 | 11 | 25 | 74 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002 | 0/0 | 855 | 29 | 27 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003 | 0/0 | 855 | 13 | 0 | 10 | 1 | 1 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004 | 0/0 | 855 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0005 | 0/0 | 855 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0006 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0007 | 0/0 | 855 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0008 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0009 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0010 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0011 | 0/0 | 855 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0012 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0013 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2568 | 120 | 12 | 24 | 61 | 7 | 16 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0002 | 0/1 | 2568 | 41 | 7 | 6 | 20 | 3 | 4 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0003 | 1/0 | 2568 | 36 | 9 | 7 | 14 | 1 | 4 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0004 | 0/0 | 2568 | 16 | 14 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0005 | 0/0 | 2568 | 12 | 0 | 9 | 1 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0006 | 0/0 | 2568 | 11 | 11 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0007 | 0/0 | 2568 | 9 | 9 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0008 | 0/0 | 2568 | 7 | 6 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0009 | 0/0 | 2568 | 6 | 5 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0010 | 0/0 | 2568 | 3 | 1 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0011 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0012 | 0/0 | 2568 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0013 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0014 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0015 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0016 | 0/0 | 2568 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0017 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0018 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0019 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0020 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0021 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0022 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0023 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0024 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0025 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0026 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0027 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0028 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0029 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0030 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0031 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0032 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0033 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0034 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| c0035 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| 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 | 1/1 | 738 | 141 | 45 | 29 | 52 | 4 | 9 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0002 | 0/0 | 738 | 123 | 24 | 25 | 47 | 8 | 19 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0003 | 0/0 | 738 | 12 | 10 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0004 | 0/0 | 738 | 10 | 9 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0005 | 0/0 | 738 | 3 | 3 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0006 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0007 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| t0008 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| 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 | 0 | 2 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2568 | 120 | 12 | 24 | 61 | 7 | 16 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0002 | 0/1 | 2568 | 41 | 7 | 6 | 20 | 3 | 4 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0003 | 1/0 | 2568 | 36 | 9 | 7 | 14 | 1 | 4 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0007 | 0/0 | 2568 | 9 | 9 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0010 | 0/0 | 2568 | 3 | 1 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0012 | 0/0 | 2568 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0016 | 0/0 | 2568 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0019 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0020 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0023 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0025 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0026 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0028 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0031 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0035 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0004 | 0/0 | 2568 | 16 | 14 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0006 | 0/0 | 2568 | 11 | 11 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0011 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003c0005 | 0/0 | 2568 | 12 | 0 | 9 | 1 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003c0017 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0008 | 0/0 | 2568 | 7 | 6 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0013 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0027 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0030 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0033 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0005c0009 | 0/0 | 2568 | 6 | 5 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0006c0014 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0007c0022 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0007c0034 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0008c0015 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0009c0018 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0010c0029 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0011c0021 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0012c0024 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0013c0032 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3305 | 41 | 3 | 7 | 27 | 2 | 2 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0001t0002 | 0/0 | 3305 | 75 | 6 | 17 | 33 | 5 | 14 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0001t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0001t0004 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0001t0008 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0002t0001 | 0/1 | 3305 | 30 | 7 | 3 | 17 | 0 | 2 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0002t0002 | 0/0 | 3305 | 10 | 0 | 2 | 3 | 3 | 2 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0002t0003 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0003t0001 | 1/0 | 3305 | 23 | 5 | 7 | 6 | 1 | 3 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0003t0002 | 0/0 | 3305 | 9 | 0 | 0 | 8 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0003t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0003t0005 | 0/0 | 3305 | 3 | 3 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0007t0001 | 0/0 | 3305 | 5 | 5 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0007t0002 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0007t0003 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0010t0001 | 0/0 | 3305 | 2 | 1 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0010t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0012t0002 | 0/0 | 3305 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0016t0002 | 0/0 | 3305 | 2 | 1 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0019t0003 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0020t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0023t0001 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0025t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0026t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0028t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0031t0007 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0001c0035t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0004t0001 | 0/0 | 3305 | 3 | 2 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0004t0002 | 0/0 | 3305 | 13 | 12 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0006t0001 | 0/0 | 3305 | 10 | 10 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0006t0006 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0002c0011t0003 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003c0005t0001 | 0/0 | 3305 | 11 | 0 | 9 | 0 | 1 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003c0005t0002 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0003c0017t0001 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0008t0001 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0008t0004 | 0/0 | 3305 | 5 | 4 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0013t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0013t0004 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0027t0002 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0030t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0004c0033t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0005c0009t0002 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0005c0009t0003 | 0/0 | 3305 | 4 | 3 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0006c0014t0001 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0007c0022t0001 | 0/0 | 3305 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0007c0034t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0008c0015t0004 | 0/0 | 3305 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0009c0018t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0010c0029t0001 | 0/0 | 3305 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0011c0021t0002 | 0/0 | 3305 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0012c0024t0001 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| a0013c0032t0002 | 0/0 | 3305 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | copy fasta | chr11 | 130154782 | 130215362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0003t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0007t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0010t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0012t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0012t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0016t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0016t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0019t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0020t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0023t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0025t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0026t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0028t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0031t0007g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0001c0035t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0006t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0011t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0002c0011t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0005t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0003c0017t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0008t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0013t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0013t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0027t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0030t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0004c0033t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0005c0009t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0006c0014t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0006c0014t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0007c0022t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0007c0034t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0008c0015t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0008c0015t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0009c0018t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0010c0029t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0011c0021t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0012c0024t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| a0013c0032t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | GBR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0188 | EUR | GBR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00323 | hp1 | a0003 | c0005 | t0001 | g0126 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0271 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00423 | hp2 | a0001 | c0010 | t0001 | g0089 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0122 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | CHS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG00735 | hp2 | a0001 | c0016 | t0002 | g0107 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0051 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01074 | hp1 | a0013 | c0032 | t0002 | g0072 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01074 | hp2 | a0001 | c0023 | t0001 | g0236 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0197 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01099 | hp2 | a0001 | c0026 | t0002 | g0136 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01106 | hp1 | a0003 | c0005 | t0001 | g0005 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01109 | hp1 | a0004 | c0008 | t0004 | g0242 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0209 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01243 | hp2 | a0003 | c0005 | t0001 | g0120 | AMR | PUR | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01255 | hp2 | a0003 | c0005 | t0001 | g0024 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01257 | hp2 | a0001 | c0012 | t0002 | g0137 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01261 | hp2 | a0005 | c0009 | t0003 | g0224 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01346 | hp1 | a0001 | c0031 | t0007 | g0027 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01496 | hp1 | a0002 | c0004 | t0002 | g0164 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0041 | EUR | IBS | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0229 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01891 | hp2 | a0002 | c0006 | t0001 | g0217 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01928 | hp2 | a0003 | c0005 | t0001 | g0127 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01934 | hp1 | a0003 | c0005 | t0001 | g0082 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01934 | hp2 | a0003 | c0005 | t0001 | g0125 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0124 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01981 | hp1 | a0009 | c0018 | t0002 | g0017 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01981 | hp2 | a0003 | c0005 | t0001 | g0123 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02004 | hp1 | a0003 | c0017 | t0001 | g0005 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02055 | hp1 | a0002 | c0004 | t0002 | g0167 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02055 | hp2 | a0002 | c0004 | t0002 | g0009 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02056 | hp1 | a0001 | c0010 | t0002 | g0084 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0097 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02145 | hp1 | a0002 | c0011 | t0003 | g0213 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02145 | hp2 | a0002 | c0006 | t0001 | g0222 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | CDX | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | CDX | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02257 | hp1 | a0008 | c0015 | t0004 | g0232 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02258 | hp2 | a0004 | c0013 | t0001 | g0253 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02280 | hp1 | a0001 | c0016 | t0002 | g0204 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0244 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0246 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02572 | hp2 | a0010 | c0029 | t0001 | g0202 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02622 | hp1 | a0004 | c0008 | t0004 | g0173 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02622 | hp2 | a0004 | c0008 | t0001 | g0174 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02630 | hp1 | a0002 | c0006 | t0006 | g0143 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02630 | hp2 | a0004 | c0008 | t0001 | g0162 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02647 | hp1 | a0001 | c0007 | t0001 | g0105 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02647 | hp2 | a0004 | c0027 | t0002 | g0255 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02717 | hp1 | a0002 | c0004 | t0002 | g0230 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02717 | hp2 | a0002 | c0006 | t0001 | g0218 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02723 | hp1 | a0005 | c0009 | t0003 | g0205 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02723 | hp2 | a0002 | c0004 | t0002 | g0009 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02809 | hp1 | a0005 | c0009 | t0003 | g0206 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0215 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02818 | hp1 | a0006 | c0014 | t0001 | g0256 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02818 | hp2 | a0001 | c0003 | t0005 | g0145 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02886 | hp2 | a0005 | c0009 | t0002 | g0220 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02895 | hp1 | a0002 | c0004 | t0002 | g0166 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02896 | hp1 | a0002 | c0004 | t0002 | g0235 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0191 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0192 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02922 | hp1 | a0006 | c0014 | t0001 | g0147 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02922 | hp2 | a0002 | c0006 | t0001 | g0157 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0163 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02965 | hp2 | a0004 | c0008 | t0004 | g0171 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0170 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0201 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02976 | hp1 | a0002 | c0004 | t0002 | g0228 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02976 | hp2 | a0001 | c0007 | t0002 | g0011 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03017 | hp1 | a0001 | c0012 | t0002 | g0001 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03017 | hp2 | a0011 | c0021 | t0002 | g0035 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03041 | hp1 | a0005 | c0009 | t0003 | g0207 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03041 | hp2 | a0001 | c0019 | t0003 | g0208 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03098 | hp1 | a0005 | c0009 | t0002 | g0223 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03139 | hp2 | a0004 | c0030 | t0001 | g0190 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03195 | hp1 | a0002 | c0004 | t0002 | g0227 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0144 | AFR | ESN | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03225 | hp2 | a0002 | c0006 | t0001 | g0214 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03453 | hp1 | a0001 | c0007 | t0002 | g0119 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03486 | hp1 | a0002 | c0006 | t0001 | g0225 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03486 | hp2 | a0001 | c0007 | t0003 | g0194 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0196 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03540 | hp2 | a0004 | c0013 | t0004 | g0238 | AFR | GWD | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03654 | hp1 | a0007 | c0022 | t0001 | g0073 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0039 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03831 | hp2 | a0003 | c0005 | t0001 | g0134 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0273 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0106 | SAS | STU | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18522 | hp2 | a0001 | c0007 | t0003 | g0193 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18906 | hp1 | a0008 | c0015 | t0004 | g0234 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0216 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18962 | hp1 | a0001 | c0025 | t0002 | g0257 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18967 | hp1 | a0003 | c0005 | t0002 | g0022 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0109 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19030 | hp1 | a0004 | c0033 | t0001 | g0175 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19030 | hp2 | a0001 | c0020 | t0001 | g0026 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19043 | hp1 | a0001 | c0028 | t0001 | g0279 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19043 | hp2 | a0004 | c0008 | t0004 | g0241 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19070 | hp2 | a0012 | c0024 | t0001 | g0037 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19240 | hp1 | a0002 | c0004 | t0002 | g0231 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA19240 | hp2 | a0007 | c0034 | t0001 | g0203 | AFR | YRI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20129 | hp1 | a0001 | c0010 | t0001 | g0025 | AFR | ASW | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20129 | hp2 | a0002 | c0004 | t0002 | g0226 | AFR | ASW | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | TSI | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0078 | SAS | GIH | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0013 | SAS | GIH | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02109 | hp1 | a0002 | c0011 | t0003 | g0212 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02559 | hp1 | a0002 | c0004 | t0002 | g0165 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0195 | AFR | ACB | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03471 | hp1 | a0004 | c0008 | t0004 | g0172 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG03471 | hp2 | a0002 | c0006 | t0001 | g0221 | AFR | MSL | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG06807 | hp1 | a0001 | c0003 | t0005 | g0146 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| HG06807 | hp2 | a0001 | c0007 | t0001 | g0118 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20300 | hp1 | a0001 | c0035 | t0001 | g0158 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | USA | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | LWK | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0069 | REF | REF | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0077 | REF | REF | ST14_chr11_130154782_130215362 | ST14 | chr11 | 130154782 | 130215362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130188542
|
G | A | 1 | a0003 | 13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/19 | 452/3305 | 254/2568 | 85/855 | chr11 | 130188542 | ||
| chr11:130189749
|
G | A | 1 | a0009 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.451G>A | p.Val151Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 649/3305 | 451/2568 | 151/855 | chr11 | 130189749 | ||
| chr11:130189752
|
A | G | 1 | a0005 | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.454A>G | p.Ile152Val | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 652/3305 | 454/2568 | 152/855 | chr11 | 130189752 | ||
| chr11:130190674
|
G | A | 1 | a0002 | 29 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(26): Show |
missense_variant | MODERATE | c.855G>A | p.Met285Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 1053/3305 | 855/2568 | 285/855 | chr11 | 130190674 | ||
| chr11:130194204
|
G | A | 1 | a0010 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.931G>A | p.Val311Ile | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/19 | 1129/3305 | 931/2568 | 311/855 | chr11 | 130194204 | ||
| chr11:130194658
|
G | A | 1 | a0011 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1034G>A | p.Arg345His | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/19 | 1232/3305 | 1034/2568 | 345/855 | chr11 | 130194658 | ||
| chr11:130194672
|
A | G | 1 | a0004 | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
missense_variant | MODERATE | c.1048A>G | p.Thr350Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/19 | 1246/3305 | 1048/2568 | 350/855 | chr11 | 130194672 | ||
| chr11:130196366
|
C | A | 2 | a0007a0008 | 4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.1141C>A | p.Arg381Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/19 | 1339/3305 | 1141/2568 | 381/855 | chr11 | 130196366 | ||
| chr11:130198991
|
G | A | 1 | a0008 | 2 | HG02257.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1729G>A | p.Gly577Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/19 | 1927/3305 | 1729/2568 | 577/855 | chr11 | 130198991 | ||
| chr11:130199999
|
C | T | 1 | a0012 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.1856C>T | p.Thr619Met | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/19 | 2054/3305 | 1856/2568 | 619/855 | chr11 | 130199999 | ||
| chr11:130208579
|
G | C | 1 | a0013 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2164G>C | p.Glu722Gln | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/19 | 2362/3305 | 2164/2568 | 722/855 | chr11 | 130208579 | ||
| chr11:130209529
|
C | T | 1 | a0006 | 2 | HG02818.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.2357C>T | p.Pro786Leu | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 18/19 | 2555/3305 | 2357/2568 | 786/855 | chr11 | 130209529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130160000
|
C | T | 1 | a0001c0035 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.21C>T | p.Arg7Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/19 | 219/3305 | 21/2568 | 7/855 | chr11 | 130160000 | ||
| chr11:130188152
|
A | G | 12 | a0001c0007a0001c0016a0001c0031others(9): Show | 34 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(31): Show |
synonymous_variant | LOW | c.120A>G | p.Pro40Pro | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/19 | 318/3305 | 120/2568 | 40/855 | chr11 | 130188152 | ||
| chr11:130188603
|
C | T | 1 | a0007c0034 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.315C>T | p.Tyr105Tyr | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/19 | 513/3305 | 315/2568 | 105/855 | chr11 | 130188603 | ||
| chr11:130189823
|
G | A | 1 | a0001c0019 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.525G>A | p.Glu175Glu | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 723/3305 | 525/2568 | 175/855 | chr11 | 130189823 | ||
| chr11:130189853
|
G | A | 1 | a0001c0020 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.555G>A | p.Ala185Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/19 | 753/3305 | 555/2568 | 185/855 | chr11 | 130189853 | ||
| chr11:130190482
|
C | T | 1 | a0001c0028 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.663C>T | p.Arg221Arg | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 861/3305 | 663/2568 | 221/855 | chr11 | 130190482 | ||
| chr11:130190617
|
G | A | 3 | a0004c0030a0006c0014a0010c0029 | 4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.798G>A | p.Ala266Ala | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 996/3305 | 798/2568 | 266/855 | chr11 | 130190617 | ||
| chr11:130190659
|
C | T | 1 | a0004c0030 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.840C>T | p.Asn280Asn | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/19 | 1038/3305 | 840/2568 | 280/855 | chr11 | 130190659 | ||
| chr11:130196440
|
C | T | 18 | a0001c0001a0001c0010a0001c0012others(15): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
synonymous_variant | LOW | c.1215C>T | p.Asn405Asn | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/19 | 1413/3305 | 1215/2568 | 405/855 | chr11 | 130196440 | ||
| chr11:130196606
|
C | T | 5 | a0004c0008a0004c0013a0004c0027others(2): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
synonymous_variant | LOW | c.1260C>T | p.Ser420Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/19 | 1458/3305 | 1260/2568 | 420/855 | chr11 | 130196606 | ||
| chr11:130197869
|
G | T | 1 | a0001c0026 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1383G>T | p.Thr461Thr | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/19 | 1581/3305 | 1383/2568 | 461/855 | chr11 | 130197869 | ||
| chr11:130198312
|
C | T | 1 | a0001c0025 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.1464C>T | p.Cys488Cys | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/19 | 1662/3305 | 1464/2568 | 488/855 | chr11 | 130198312 | ||
| chr11:130198390
|
C | T | 3 | a0004c0008a0004c0013a0004c0030 | 10 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1542C>T | p.Cys514Cys | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/19 | 1740/3305 | 1542/2568 | 514/855 | chr11 | 130198390 | ||
| chr11:130198596
|
G | C | 5 | a0001c0002a0001c0010a0001c0020others(2): Show | 48 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(45): Show |
synonymous_variant | LOW | c.1659G>C | p.Gly553Gly | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/19 | 1857/3305 | 1659/2568 | 553/855 | chr11 | 130198596 | ||
| chr11:130199026
|
C | T | 1 | a0003c0017 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.1764C>T | p.Asp588Asp | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/19 | 1962/3305 | 1764/2568 | 588/855 | chr11 | 130199026 | ||
| chr11:130209679
|
C | T | 1 | a0001c0012 | 2 | HG01257.hp2 HG03017.hp1 |
synonymous_variant | LOW | c.2424C>T | p.Pro808Pro | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 2622/3305 | 2424/2568 | 808/855 | chr11 | 130209679 | ||
| chr11:130209688
|
C | T | 1 | a0001c0023 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.2433C>T | p.Ser811Ser | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 2631/3305 | 2433/2568 | 811/855 | chr11 | 130209688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130159881
|
T | C | 2 | a0001c0003t0005a0002c0006t0006 | 4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-99T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/19 | 99 | chr11 | 130159881 | |||||
| chr11:130210024
|
G | C | 1 | a0001c0031t0007 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 201 | chr11 | 130210024 | |||||
| chr11:130210088
|
C | G | 1 | a0001c0001t0008 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 265 | chr11 | 130210088 | |||||
| chr11:130210122
|
C | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*299C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 299 | chr11 | 130210122 | |||||
| chr11:130210142
|
C | G | 17 | a0001c0001t0002a0001c0001t0008a0001c0002t0002others(14): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 319 | chr11 | 130210142 | |||||
| chr11:130210170
|
G | A | 17 | a0001c0001t0002a0001c0001t0008a0001c0002t0002others(14): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*347G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 347 | chr11 | 130210170 | |||||
| chr11:130210313
|
C | T | 4 | a0001c0001t0004a0004c0008t0004a0004c0013t0004others(1): Show | 10 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*490C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 19/19 | 490 | chr11 | 130210313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130160143
|
C | T | 30 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(27): Show | 31 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.81+83C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160143 | ||||||
| chr11:130160198
|
C | G | 2 | a0001c0001t0001g0252a0001c0001t0002g0251 | 2 | NA18979.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.81+138C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160198 | ||||||
| chr11:130160468
|
C | G | 120 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0269others(117): Show | 122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.81+408C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160468 | ||||||
| chr11:130160487
|
T | A | 1 | a0004c0008t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.81+427T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160487 | ||||||
| chr11:130160668
|
A | T | 1 | a0001c0001t0002g0161 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.81+608A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160668 | ||||||
| chr11:130160677
|
G | C | 1 | a0004c0013t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+617G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160677 | ||||||
| chr11:130160876
|
A | G | 1 | a0001c0001t0002g0281 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.81+816A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130160876 | ||||||
| chr11:130161044
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.81+984C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161044 | ||||||
| chr11:130161391
|
AC | A | 37 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.81+1333delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130161391 | |||||
| chr11:130161565
|
T | A | 15 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(12): Show | 15 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+1505T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161565 | ||||||
| chr11:130161584
|
AC | A | 15 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0254others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+1529delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130161584 | |||||
| chr11:130161740
|
G | A | 1 | a0001c0007t0002g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+1680G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161740 | ||||||
| chr11:130161934
|
A | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0148others(136): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+1874A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161934 | ||||||
| chr11:130161970
|
C | G | 4 | a0001c0001t0001g0139a0001c0001t0002g0140a0001c0001t0002g0141others(1): Show | 4 | HG02615.hp1 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1910C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130161970 | ||||||
| chr11:130162195
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.81+2135A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162195 | ||||||
| chr11:130162250
|
G | A | 1 | a0004c0030t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.81+2190G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162250 | ||||||
| chr11:130162590
|
T | C | 4 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2530T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162590 | ||||||
| chr11:130162628
|
A | G | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+2568A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162628 | ||||||
| chr11:130162771
|
C | G | 3 | a0001c0001t0002g0135a0001c0012t0002g0137a0001c0026t0002g0136 | 3 | HG01099.hp2 HG01257.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+2711C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162771 | ||||||
| chr11:130162773
|
A | G | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2713A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162773 | ||||||
| chr11:130162822
|
C | G | 1 | a0003c0005t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+2762C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162822 | ||||||
| chr11:130162940
|
T | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0148others(74): Show | 80 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.81+2880T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130162940 | ||||||
| chr11:130163121
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81+3061C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163121 | ||||||
| chr11:130163122
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81+3062G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163122 | ||||||
| chr11:130163675
|
G | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+3615G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163675 | ||||||
| chr11:130163722
|
C | G | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+3662C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163722 | ||||||
| chr11:130163785
|
G | A | 5 | a0002c0004t0002g0163a0002c0004t0002g0164a0002c0004t0002g0165others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+3725G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163785 | ||||||
| chr11:130163975
|
A | G | 36 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(33): Show | 37 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.81+3915A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130163975 | ||||||
| chr11:130164021
|
C | G | 1 | a0001c0023t0001g0236 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+3961C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164021 | ||||||
| chr11:130164082
|
C | T | 1 | a0001c0002t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+4022C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164082 | ||||||
| chr11:130164252
|
G | A | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+4192G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164252 | ||||||
| chr11:130164281
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0148others(1): Show | 6 | HG00408.hp1 NA18969.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+4221T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164281 | ||||||
| chr11:130164284
|
T | C | 1 | a0002c0004t0001g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+4224T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164284 | ||||||
| chr11:130164427
|
T | C | 1 | a0001c0003t0001g0013 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+4367T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164427 | ||||||
| chr11:130164529
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+4469C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164529 | ||||||
| chr11:130164636
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+4576C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164636 | ||||||
| chr11:130164683
|
T | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+4623T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164683 | ||||||
| chr11:130164718
|
C | CTTA | 25 | a0001c0001t0001g0280a0001c0001t0002g0020a0001c0001t0002g0021others(22): Show | 26 | HG01243.hp1 HG01261.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+4691_81+4693dup others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
C | CTTATTA | 19 | a0001c0001t0001g0016a0001c0001t0002g0015a0001c0001t0004g0199others(16): Show | 19 | HG00597.hp2 HG00673.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+4688_81+4693dup others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
C | CTTATTAT others(2): Show |
36 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0002g0182others(33): Show | 36 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+4685_81+4693dup others(9): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
C | CTTATTAT others(5): Show |
29 | a0001c0001t0002g0260a0001c0001t0003g0247a0001c0002t0001g0168others(26): Show | 29 | HG00423.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+4682_81+4693dup others(12): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
C | CTTATTAT others(8): Show |
3 | a0001c0001t0001g0237a0004c0027t0002g0255a0007c0034t0001g0203 | 3 | HG02109.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.81+4679_81+4693dup others(15): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
CTTA | C | 5 | a0002c0004t0002g0163a0002c0004t0002g0164a0002c0004t0002g0165others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+4691_81+4693del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
CTTATTA | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0148a0001c0001t0001g0233others(10): Show | 15 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+4688_81+4693del others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164718
|
CTTATTAT others(2): Show |
C | 11 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0131others(8): Show | 13 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+4685_81+4693del others(9): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130164718 | |||||
| chr11:130164794
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+4734A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164794 | ||||||
| chr11:130164841
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.81+4781G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164841 | ||||||
| chr11:130164844
|
T | A | 1 | a0001c0028t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+4784T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164844 | ||||||
| chr11:130164894
|
T | A | 19 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(16): Show | 19 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+4834T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164894 | ||||||
| chr11:130164989
|
G | A | 1 | a0003c0005t0001g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.81+4929G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130164989 | ||||||
| chr11:130165000
|
G | A | 14 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(11): Show | 14 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+4940G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165000 | ||||||
| chr11:130165110
|
C | T | 1 | a0004c0033t0001g0175 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+5050C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165110 | ||||||
| chr11:130165190
|
C | T | 64 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(61): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.81+5130C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165190 | ||||||
| chr11:130165204
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81+5144C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165204 | ||||||
| chr11:130165290
|
T | A | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.81+5230T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165290 | ||||||
| chr11:130165387
|
G | A | 2 | a0001c0002t0001g0168a0001c0003t0001g0169 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.81+5327G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165387 | ||||||
| chr11:130165410
|
G | A | 2 | a0001c0001t0001g0156a0001c0010t0001g0025 | 2 | HG01069.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.81+5350G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165410 | ||||||
| chr11:130165560
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.81+5500T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165560 | ||||||
| chr11:130165703
|
C | T | 63 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(60): Show | 64 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+5643C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130165703 | ||||||
| chr11:130166099
|
G | A | 1 | a0001c0020t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81+6039G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166099 | ||||||
| chr11:130166310
|
T | A | 1 | a0001c0002t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+6250T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166310 | ||||||
| chr11:130166476
|
C | T | 1 | a0001c0003t0001g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+6416C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166476 | ||||||
| chr11:130166749
|
T | C | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+6689T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166749 | ||||||
| chr11:130166791
|
G | A | 1 | a0001c0031t0007g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.81+6731G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166791 | ||||||
| chr11:130166932
|
C | T | 1 | a0001c0003t0005g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81+6872C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166932 | ||||||
| chr11:130166939
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+6879G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166939 | ||||||
| chr11:130166963
|
C | T | 17 | a0001c0001t0001g0128a0001c0001t0002g0129a0001c0001t0002g0182others(14): Show | 17 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+6903C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166963 | ||||||
| chr11:130166982
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+6922C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130166982 | ||||||
| chr11:130167121
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+7061G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167121 | ||||||
| chr11:130167212
|
A | G | 20 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0003t0001g0219others(17): Show | 20 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+7152A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167212 | ||||||
| chr11:130167218
|
A | T | 1 | a0004c0033t0001g0175 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+7158A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167218 | ||||||
| chr11:130167273
|
G | C | 1 | a0001c0001t0002g0160 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.81+7213G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167273 | ||||||
| chr11:130167301
|
A | T | 13 | a0001c0001t0001g0121a0003c0005t0001g0005a0003c0005t0001g0024others(10): Show | 13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+7241A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167301 | ||||||
| chr11:130167427
|
T | A | 1 | a0001c0003t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+7367T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167427 | ||||||
| chr11:130167767
|
T | G | 1 | a0001c0001t0002g0254 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.81+7707T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167767 | ||||||
| chr11:130167778
|
G | A | 3 | a0001c0003t0001g0209a0001c0019t0003g0208a0001c0023t0001g0236 | 3 | HG01074.hp2 HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+7718G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167778 | ||||||
| chr11:130167807
|
C | T | 2 | a0001c0001t0001g0156a0001c0010t0001g0025 | 2 | HG01069.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.81+7747C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130167807 | ||||||
| chr11:130168008
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.81+7948C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168008 | ||||||
| chr11:130168010
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.81+7950C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168010 | ||||||
| chr11:130168081
|
G | C | 141 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 146 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.81+8021G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168081 | ||||||
| chr11:130168132
|
A | G | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+8072A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168132 | ||||||
| chr11:130168479
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.81+8419G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168479 | ||||||
| chr11:130168592
|
A | C | 121 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.81+8532A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168592 | ||||||
| chr11:130168829
|
C | A | 4 | a0001c0002t0001g0210a0001c0002t0001g0211a0002c0011t0003g0212others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+8769C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168829 | ||||||
| chr11:130168960
|
T | C | 1 | a0001c0002t0002g0248 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+8900T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130168960 | ||||||
| chr11:130169034
|
TA | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.81+8983delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169034 | |||||
| chr11:130169063
|
C | T | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+9003C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169063 | ||||||
| chr11:130169075
|
T | C | 1 | a0001c0002t0001g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+9015T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169075 | ||||||
| chr11:130169091
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.81+9031G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169091 | ||||||
| chr11:130169092
|
G | GT | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0110others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.81+9054dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169092
|
G | GTT | 19 | a0001c0001t0001g0115a0001c0003t0001g0170a0001c0003t0002g0116others(16): Show | 19 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+9053_81+9054dup others(2): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169092
|
G | GTTT | 6 | a0001c0003t0005g0144a0001c0003t0005g0145a0001c0003t0005g0146others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+9052_81+9054dup others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169092
|
GT | G | 38 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0276others(35): Show | 39 | HG00621.hp2 HG01243.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.81+9054delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169092
|
GTT | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.81+9053_81+9054del others(2): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169092
|
GTTT | G | 11 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0002t0001g0210others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+9052_81+9054del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130169092 | |||||
| chr11:130169153
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+9093G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169153 | ||||||
| chr11:130169382
|
A | C | 2 | a0001c0001t0001g0094a0001c0001t0002g0093 | 2 | NA18959.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.81+9322A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169382 | ||||||
| chr11:130169518
|
C | T | 20 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0003t0001g0219others(17): Show | 20 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+9458C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169518 | ||||||
| chr11:130169605
|
G | A | 15 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(12): Show | 15 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+9545G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169605 | ||||||
| chr11:130169698
|
G | A | 1 | a0011c0021t0002g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+9638G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130169698 | ||||||
| chr11:130170231
|
C | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0012c0024t0001g0037 | 3 | NA18940.hp2 NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.81+10171C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170231 | ||||||
| chr11:130170331
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.81+10271G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170331 | ||||||
| chr11:130170610
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0002g0093 | 2 | NA18959.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.81+10550G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170610 | ||||||
| chr11:130170644
|
GGGTTCCT others(23): Show |
G | 1 | a0002c0004t0002g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+10595_81+10624d others(32): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130170644 | |||||
| chr11:130170718
|
C | T | 1 | a0005c0009t0003g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.81+10658C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170718 | ||||||
| chr11:130170758
|
G | C | 1 | a0002c0004t0002g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.81+10698G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130170758 | ||||||
| chr11:130171049
|
A | G | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+10989A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171049 | ||||||
| chr11:130171268
|
C | T | 1 | a0001c0002t0001g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.81+11208C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171268 | ||||||
| chr11:130171311
|
T | C | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+11251T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171311 | ||||||
| chr11:130171339
|
C | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 36 | HG00408.hp1 HG00438.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+11279C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171339 | ||||||
| chr11:130171362
|
C | A | 2 | a0004c0013t0001g0253a0004c0027t0002g0255 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.81+11302C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171362 | ||||||
| chr11:130171555
|
G | A | 1 | a0001c0035t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+11495G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171555 | ||||||
| chr11:130171586
|
G | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 36 | HG00408.hp1 HG00438.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+11526G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171586 | ||||||
| chr11:130171652
|
T | C | 1 | a0001c0023t0001g0236 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+11592T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171652 | ||||||
| chr11:130171660
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.81+11600A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171660 | ||||||
| chr11:130171760
|
C | A | 2 | a0004c0008t0001g0162a0004c0008t0001g0174 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.81+11700C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171760 | ||||||
| chr11:130171961
|
G | A | 16 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0002g0240others(13): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+11901G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130171961 | ||||||
| chr11:130172145
|
C | T | 132 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 136 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.81+12085C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172145 | ||||||
| chr11:130172170
|
A | T | 1 | a0001c0001t0002g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.81+12110A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172170 | ||||||
| chr11:130172216
|
G | A | 1 | a0001c0003t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.81+12156G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172216 | ||||||
| chr11:130172274
|
T | A | 5 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(2): Show | 5 | HG01884.hp2 HG02040.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+12214T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172274 | ||||||
| chr11:130172275
|
A | T | 2 | a0001c0001t0002g0090a0001c0001t0002g0114 | 2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.81+12215A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172275 | ||||||
| chr11:130172411
|
C | CT | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0110others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+12375dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130172411 | |||||
| chr11:130172411
|
CT | C | 70 | a0001c0001t0001g0042a0001c0001t0001g0128a0001c0001t0001g0269others(67): Show | 72 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.81+12375delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130172411 | |||||
| chr11:130172486
|
C | T | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+12426C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172486 | ||||||
| chr11:130172487
|
G | C | 1 | a0001c0002t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.81+12427G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172487 | ||||||
| chr11:130172518
|
C | T | 1 | a0002c0006t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.81+12458C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172518 | ||||||
| chr11:130172527
|
C | T | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+12467C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172527 | ||||||
| chr11:130172568
|
C | T | 3 | a0001c0003t0002g0108a0001c0003t0002g0109a0001c0003t0002g0117 | 3 | NA18982.hp1 NA19000.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.81+12508C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172568 | ||||||
| chr11:130172707
|
G | A | 1 | a0011c0021t0002g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+12647G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172707 | ||||||
| chr11:130172915
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.81+12855G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172915 | ||||||
| chr11:130172964
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.81+12904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172964 | ||||||
| chr11:130172964
|
G | T | 34 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(31): Show | 35 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.81+12904G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130172964 | ||||||
| chr11:130173058
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.81+12998G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173058 | ||||||
| chr11:130173360
|
G | A | 1 | a0004c0013t0004g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+13300G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173360 | ||||||
| chr11:130173431
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 66 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.81+13371G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173431 | ||||||
| chr11:130173572
|
C | T | 3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | NA18941.hp1 NA18962.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.81+13512C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173572 | ||||||
| chr11:130173595
|
C | CA | 22 | a0001c0001t0001g0110a0001c0001t0001g0138a0001c0001t0001g0233others(19): Show | 23 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+13551dupA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130173595 | |||||
| chr11:130173595
|
CA | C | 28 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(25): Show | 29 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.81+13551delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130173595 | |||||
| chr11:130173685
|
G | A | 34 | a0001c0001t0001g0128a0001c0001t0002g0030a0001c0001t0002g0129others(31): Show | 34 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.81+13625G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173685 | ||||||
| chr11:130173894
|
C | G | 1 | a0001c0001t0002g0021 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.81+13834C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130173894 | ||||||
| chr11:130174020
|
G | C | 1 | a0002c0004t0001g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+13960G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174020 | ||||||
| chr11:130174083
|
A | G | 12 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(9): Show | 12 | HG01074.hp2 HG01261.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+14023A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174083 | ||||||
| chr11:130174336
|
A | T | 35 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.82-13778A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174336 | ||||||
| chr11:130174340
|
G | T | 24 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(21): Show | 24 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-13774G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174340 | ||||||
| chr11:130174520
|
G | T | 35 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.82-13594G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174520 | ||||||
| chr11:130174592
|
A | G | 4 | a0001c0003t0005g0144a0001c0003t0005g0145a0001c0003t0005g0146others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-13522A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174592 | ||||||
| chr11:130174614
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-13500T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174614 | ||||||
| chr11:130174988
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-13126G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130174988 | ||||||
| chr11:130175138
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-12976C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175138 | ||||||
| chr11:130175139
|
G | A | 1 | a0006c0014t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82-12975G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175139 | ||||||
| chr11:130175205
|
G | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.82-12909G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175205 | ||||||
| chr11:130175219
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-12895T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175219 | ||||||
| chr11:130175303
|
G | GT | 9 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0002g0260others(6): Show | 9 | HG01123.hp1 HG01496.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-12802dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130175303 | |||||
| chr11:130175303
|
G | T | 1 | a0001c0020t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-12811G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175303 | ||||||
| chr11:130175304
|
T | G | 2 | a0001c0002t0001g0168a0001c0003t0001g0169 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.82-12810T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175304 | ||||||
| chr11:130175440
|
C | T | 4 | a0005c0009t0003g0205a0005c0009t0003g0206a0005c0009t0003g0207others(1): Show | 4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-12674C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175440 | ||||||
| chr11:130175540
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-12574C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175540 | ||||||
| chr11:130175601
|
A | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.82-12513A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175601 | ||||||
| chr11:130175871
|
C | A | 1 | a0001c0001t0002g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.82-12243C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175871 | ||||||
| chr11:130175897
|
A | G | 2 | a0001c0003t0001g0219a0002c0006t0001g0225 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.82-12217A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175897 | ||||||
| chr11:130175912
|
C | T | 1 | a0002c0006t0001g0222 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.82-12202C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130175912 | ||||||
| chr11:130176033
|
G | A | 1 | a0004c0008t0004g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-12081G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176033 | ||||||
| chr11:130176044
|
C | T | 14 | a0001c0002t0001g0168a0001c0003t0001g0169a0001c0003t0001g0170others(11): Show | 14 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-12070C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176044 | ||||||
| chr11:130176083
|
G | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.82-12031G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176083 | ||||||
| chr11:130176247
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.82-11867T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176247 | ||||||
| chr11:130176328
|
G | T | 1 | a0001c0001t0002g0254 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.82-11786G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176328 | ||||||
| chr11:130176370
|
CT | C | 8 | a0001c0001t0001g0154a0001c0001t0002g0033a0001c0001t0002g0142others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-11732delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176370 | |||||
| chr11:130176493
|
G | A | 69 | a0001c0001t0001g0128a0001c0001t0001g0269a0001c0001t0001g0276others(66): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.82-11621G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176493 | ||||||
| chr11:130176683
|
C | T | 3 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0033t0001g0175 | 3 | HG02622.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.82-11431C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176683 | ||||||
| chr11:130176788
|
C | CT | 25 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0110others(22): Show | 25 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-11298dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176788
|
CT | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0092others(51): Show | 56 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.82-11298delT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176788
|
CTT | C | 40 | a0001c0001t0001g0131a0001c0001t0001g0269a0001c0001t0001g0276others(37): Show | 41 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-11299_82-11298d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176788
|
CTTT | C | 17 | a0001c0003t0001g0169a0001c0003t0001g0170a0001c0003t0001g0250others(14): Show | 17 | HG01496.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-11300_82-11298d others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176788
|
CTTTTTTT others(4): Show |
C | 11 | a0001c0001t0001g0233a0001c0003t0001g0219a0002c0004t0002g0009others(8): Show | 12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-11308_82-11298d others(13): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176788
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0004t0002g0235 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.82-11309_82-11298d others(14): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130176788 | |||||
| chr11:130176821
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-11293C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176821 | ||||||
| chr11:130176954
|
G | A | 1 | a0002c0004t0002g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82-11160G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130176954 | ||||||
| chr11:130177014
|
G | C | 34 | a0001c0001t0001g0128a0001c0001t0002g0030a0001c0001t0002g0129others(31): Show | 34 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.82-11100G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177014 | ||||||
| chr11:130177033
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.82-11081C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177033 | ||||||
| chr11:130177097
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0002t0001g0210others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-11017G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177097 | ||||||
| chr11:130177254
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.82-10860C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177254 | ||||||
| chr11:130177569
|
C | A | 117 | a0001c0001t0001g0128a0001c0001t0001g0237a0001c0001t0001g0269others(114): Show | 118 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.82-10545C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177569 | ||||||
| chr11:130177779
|
GAA | G | 4 | a0002c0004t0002g0164a0002c0004t0002g0165a0002c0004t0002g0166others(1): Show | 4 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-10334_82-10333d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177779 | ||||||
| chr11:130177910
|
G | C | 5 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-10204G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130177910 | ||||||
| chr11:130178050
|
T | C | 1 | a0007c0034t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82-10064T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178050 | ||||||
| chr11:130178091
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.82-10023A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178091 | ||||||
| chr11:130178125
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-9989T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178125 | ||||||
| chr11:130178151
|
C | T | 1 | a0002c0004t0001g0197 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-9963C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178151 | ||||||
| chr11:130178392
|
T | TTATGGCC others(121): Show |
106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.82-9720_82-9719ins others(128): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130178392 | |||||
| chr11:130178392
|
T | TTATGGCC others(121): Show |
37 | a0001c0001t0001g0128a0001c0001t0002g0030a0001c0001t0002g0129others(34): Show | 37 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.82-9720_82-9719ins others(128): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130178392 | |||||
| chr11:130178506
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.82-9608C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178506 | ||||||
| chr11:130178530
|
G | T | 1 | a0001c0028t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-9584G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178530 | ||||||
| chr11:130178871
|
G | T | 14 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0003t0001g0219others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-9243G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178871 | ||||||
| chr11:130178962
|
C | G | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82-9152C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178962 | ||||||
| chr11:130178979
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.82-9135C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130178979 | ||||||
| chr11:130179931
|
G | A | 1 | a0001c0003t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.82-8183G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130179931 | ||||||
| chr11:130180000
|
G | C | 1 | a0001c0002t0001g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.82-8114G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180000 | ||||||
| chr11:130180000
|
G | T | 1 | a0002c0006t0001g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-8114G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180000 | ||||||
| chr11:130180048
|
G | T | 1 | a0001c0002t0001g0263 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.82-8066G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180048 | ||||||
| chr11:130180097
|
C | T | 1 | a0001c0003t0002g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-8017C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180097 | ||||||
| chr11:130180155
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 16 | HG00408.hp1 HG00438.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-7959C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180155 | ||||||
| chr11:130180483
|
G | C | 1 | a0003c0005t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82-7631G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180483 | ||||||
| chr11:130180593
|
G | A | 1 | a0002c0006t0001g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.82-7521G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180593 | ||||||
| chr11:130180845
|
G | A | 1 | a0001c0023t0001g0236 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.82-7269G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180845 | ||||||
| chr11:130180927
|
G | A | 130 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0023others(127): Show | 134 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.82-7187G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180927 | ||||||
| chr11:130180988
|
C | A | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-7126C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130180988 | ||||||
| chr11:130181117
|
TGTCCCTG others(18): Show |
T | 2 | a0004c0008t0004g0241a0004c0008t0004g0242 | 2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82-6976_82-6952del others(25): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130181117 | |||||
| chr11:130181210
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.82-6904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181210 | ||||||
| chr11:130181245
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.82-6869G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181245 | ||||||
| chr11:130181261
|
G | A | 1 | a0001c0003t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.82-6853G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181261 | ||||||
| chr11:130181270
|
C | T | 29 | a0001c0001t0001g0128a0001c0001t0002g0030a0001c0001t0002g0182others(26): Show | 29 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.82-6844C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181270 | ||||||
| chr11:130181285
|
C | T | 4 | a0001c0003t0005g0144a0001c0003t0005g0145a0001c0003t0005g0146others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-6829C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181285 | ||||||
| chr11:130181365
|
G | A | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-6749G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181365 | ||||||
| chr11:130181455
|
C | T | 1 | a0007c0034t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82-6659C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181455 | ||||||
| chr11:130181652
|
C | T | 34 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(31): Show | 35 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.82-6462C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181652 | ||||||
| chr11:130181772
|
T | C | 2 | a0002c0004t0001g0195a0010c0029t0001g0202 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.82-6342T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181772 | ||||||
| chr11:130181773
|
G | A | 2 | a0001c0001t0002g0028a0007c0022t0001g0073 | 2 | HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.82-6341G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181773 | ||||||
| chr11:130181957
|
T | C | 282 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(279): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.82-6157T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130181957 | ||||||
| chr11:130182004
|
C | T | 29 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(26): Show | 30 | HG00621.hp2 HG00642.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-6110C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182004 | ||||||
| chr11:130182057
|
A | G | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-6057A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182057 | ||||||
| chr11:130182114
|
A | G | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.82-6000A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182114 | ||||||
| chr11:130182309
|
G | GT | 3 | a0001c0003t0005g0144a0001c0003t0005g0145a0001c0003t0005g0146 | 3 | HG02818.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-5802dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130182309 | |||||
| chr11:130182360
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.82-5754C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182360 | ||||||
| chr11:130182361
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.82-5753G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182361 | ||||||
| chr11:130182385
|
G | C | 26 | a0001c0001t0001g0233a0001c0002t0001g0210a0001c0002t0001g0211others(23): Show | 27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-5729G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182385 | ||||||
| chr11:130182417
|
G | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 45 | HG00408.hp1 HG00438.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.82-5697G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182417 | ||||||
| chr11:130182448
|
G | A | 1 | a0001c0016t0002g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.82-5666G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182448 | ||||||
| chr11:130182514
|
T | C | 250 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.82-5600T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182514 | ||||||
| chr11:130182528
|
C | T | 26 | a0001c0001t0001g0233a0001c0002t0001g0210a0001c0002t0001g0211others(23): Show | 27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-5586C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182528 | ||||||
| chr11:130182566
|
C | T | 1 | a0010c0029t0001g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82-5548C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182566 | ||||||
| chr11:130182567
|
G | A | 4 | a0001c0003t0005g0144a0001c0003t0005g0145a0001c0003t0005g0146others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-5547G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182567 | ||||||
| chr11:130182652
|
C | CT | 36 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0280others(33): Show | 37 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.82-5447dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130182652 | |||||
| chr11:130182701
|
G | A | 3 | a0001c0003t0001g0219a0002c0006t0001g0157a0002c0006t0001g0229 | 3 | HG01891.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.82-5413G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182701 | ||||||
| chr11:130182731
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.82-5383T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182731 | ||||||
| chr11:130182731
|
T | G | 1 | a0001c0003t0002g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-5383T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182731 | ||||||
| chr11:130182733
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-5381T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182733 | ||||||
| chr11:130182750
|
A | G | 4 | a0001c0003t0001g0198a0001c0016t0002g0107a0001c0031t0007g0027others(1): Show | 4 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-5364A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182750 | ||||||
| chr11:130182825
|
G | A | 188 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.82-5289G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182825 | ||||||
| chr11:130182849
|
C | G | 1 | a0001c0001t0002g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.82-5265C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182849 | ||||||
| chr11:130182908
|
C | T | 2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.82-5206C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182908 | ||||||
| chr11:130182941
|
C | T | 2 | a0001c0023t0001g0236a0001c0035t0001g0158 | 2 | HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.82-5173C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130182941 | ||||||
| chr11:130183017
|
C | T | 1 | a0001c0001t0002g0251 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.82-5097C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183017 | ||||||
| chr11:130183131
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.82-4983T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183131 | ||||||
| chr11:130183392
|
G | A | 31 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0003t0001g0170others(28): Show | 32 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-4722G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183392 | ||||||
| chr11:130183476
|
T | C | 268 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(265): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.82-4638T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183476 | ||||||
| chr11:130183542
|
TA | T | 64 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0001t0001g0096others(61): Show | 65 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.82-4553delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130183542 | |||||
| chr11:130183673
|
C | T | 31 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0003t0001g0170others(28): Show | 32 | HG01099.hp1 HG01496.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-4441C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183673 | ||||||
| chr11:130183687
|
A | T | 1 | a0001c0019t0003g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-4427A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183687 | ||||||
| chr11:130183744
|
T | A | 9 | a0001c0007t0001g0105a0001c0007t0001g0118a0001c0007t0001g0201others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-4370T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183744 | ||||||
| chr11:130183824
|
C | T | 1 | a0001c0003t0001g0198 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.82-4290C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130183824 | ||||||
| chr11:130184148
|
A | G | 12 | a0001c0007t0001g0105a0001c0007t0001g0118a0001c0007t0001g0201others(9): Show | 12 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-3966A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184148 | ||||||
| chr11:130184169
|
C | A | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3945C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184169 | ||||||
| chr11:130184495
|
G | A | 30 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0002g0260others(27): Show | 31 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.82-3619G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184495 | ||||||
| chr11:130184530
|
C | G | 1 | a0001c0001t0002g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-3584C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184530 | ||||||
| chr11:130184565
|
T | C | 8 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(5): Show | 8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-3549T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184565 | ||||||
| chr11:130184737
|
T | C | 1 | a0001c0003t0002g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-3377T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184737 | ||||||
| chr11:130184873
|
G | A | 1 | a0001c0002t0001g0249 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.82-3241G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184873 | ||||||
| chr11:130184882
|
A | G | 2 | a0001c0001t0001g0233a0002c0004t0001g0196 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.82-3232A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184882 | ||||||
| chr11:130184938
|
A | G | 12 | a0001c0007t0001g0105a0001c0007t0001g0118a0001c0007t0001g0201others(9): Show | 12 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-3176A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184938 | ||||||
| chr11:130184986
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-3128C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184986 | ||||||
| chr11:130184987
|
C | T | 3 | a0001c0001t0002g0133a0003c0005t0001g0126a0003c0005t0001g0134 | 3 | HG00323.hp1 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.82-3127C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130184987 | ||||||
| chr11:130185081
|
C | G | 1 | a0001c0019t0003g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-3033C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185081 | ||||||
| chr11:130185221
|
A | C | 33 | a0001c0007t0001g0105a0001c0007t0001g0118a0001c0007t0001g0191others(30): Show | 33 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-2893A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185221 | ||||||
| chr11:130185323
|
G | A | 1 | a0006c0014t0001g0256 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-2791G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185323 | ||||||
| chr11:130185525
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-2589G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185525 | ||||||
| chr11:130185528
|
C | A | 1 | a0001c0001t0002g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-2586C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185528 | ||||||
| chr11:130185671
|
C | T | 8 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(5): Show | 8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-2443C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185671 | ||||||
| chr11:130185713
|
T | C | 110 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0001g0269others(107): Show | 112 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.82-2401T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185713 | ||||||
| chr11:130185730
|
G | T | 6 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0003t0003g0246others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-2384G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185730 | ||||||
| chr11:130185868
|
C | T | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.82-2246C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185868 | ||||||
| chr11:130185911
|
G | A | 4 | a0005c0009t0003g0205a0005c0009t0003g0206a0005c0009t0003g0207others(1): Show | 4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-2203G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185911 | ||||||
| chr11:130185924
|
C | T | 1 | a0001c0003t0001g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-2190C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185924 | ||||||
| chr11:130185954
|
C | T | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82-2160C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185954 | ||||||
| chr11:130185955
|
G | A | 2 | a0002c0011t0003g0212a0002c0011t0003g0213 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.82-2159G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130185955 | ||||||
| chr11:130186059
|
C | T | 5 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-2055C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186059 | ||||||
| chr11:130186223
|
CA | C | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1885delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130186223 | |||||
| chr11:130186342
|
A | C | 44 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0001t0004g0199others(41): Show | 44 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.82-1772A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186342 | ||||||
| chr11:130186479
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.82-1635A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186479 | ||||||
| chr11:130186503
|
A | G | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-1611A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186503 | ||||||
| chr11:130186618
|
A | G | 1 | a0010c0029t0001g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82-1496A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186618 | ||||||
| chr11:130186787
|
C | T | 4 | a0005c0009t0003g0205a0005c0009t0003g0206a0005c0009t0003g0207others(1): Show | 4 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1327C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186787 | ||||||
| chr11:130186949
|
A | G | 5 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-1165A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130186949 | ||||||
| chr11:130187073
|
C | T | 1 | a0001c0010t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.82-1041C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187073 | ||||||
| chr11:130187184
|
G | A | 8 | a0001c0001t0001g0055a0001c0001t0002g0036a0001c0001t0002g0038others(5): Show | 8 | NA18940.hp2 NA18944.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-930G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187184 | ||||||
| chr11:130187191
|
A | AG | 4 | a0001c0007t0001g0118a0001c0007t0001g0201a0001c0007t0002g0011others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-922dupG | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 130187191 | |||||
| chr11:130187369
|
C | G | 1 | a0003c0005t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.82-745C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187369 | ||||||
| chr11:130187794
|
C | T | 3 | a0007c0034t0001g0203a0008c0015t0004g0232a0008c0015t0004g0234 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.82-320C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187794 | ||||||
| chr11:130187839
|
C | A | 1 | a0001c0019t0003g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-275C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187839 | ||||||
| chr11:130187864
|
T | G | 4 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-250T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187864 | ||||||
| chr11:130187916
|
G | T | 8 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(5): Show | 8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-198G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130187916 | ||||||
| chr11:130188002
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0085 | 2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.82-112C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130188002 | ||||||
| chr11:130188097
|
C | T | 4 | a0004c0030t0001g0190a0006c0014t0001g0147a0006c0014t0001g0256others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-17C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 1/18 | chr11 | 130188097 | ||||||
| chr11:130188295
|
T | C | 9 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(6): Show | 9 | HG02280.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+22T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188295 | ||||||
| chr11:130188297
|
C | T | 8 | a0001c0019t0003g0208a0005c0009t0003g0205a0005c0009t0003g0206others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+24C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188297 | ||||||
| chr11:130188325
|
C | T | 1 | a0001c0007t0001g0201 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241+52C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188325 | ||||||
| chr11:130188371
|
G | A | 3 | a0001c0016t0002g0107a0001c0031t0007g0027a0013c0032t0002g0072 | 3 | HG00735.hp2 HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241+98G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188371 | ||||||
| chr11:130188467
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242-63C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188467 | ||||||
| chr11:130188511
|
G | A | 8 | a0001c0019t0003g0208a0005c0009t0003g0205a0005c0009t0003g0206others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-19G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 2/18 | chr11 | 130188511 | ||||||
| chr11:130188697
|
G | A | 4 | a0001c0007t0001g0191a0001c0007t0001g0192a0001c0007t0003g0193others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+40G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188697 | ||||||
| chr11:130188754
|
T | C | 3 | a0001c0001t0001g0237a0001c0001t0002g0240a0001c0002t0001g0239 | 3 | HG01884.hp2 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.369+97T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188754 | ||||||
| chr11:130188790
|
T | C | 3 | a0007c0034t0001g0203a0008c0015t0004g0232a0008c0015t0004g0234 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.370-79T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 3/18 | chr11 | 130188790 | ||||||
| chr11:130189040
|
G | A | 1 | a0004c0030t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440+101G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189040 | ||||||
| chr11:130189040
|
G | T | 1 | a0001c0007t0001g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.440+101G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189040 | ||||||
| chr11:130189043
|
C | T | 16 | a0001c0001t0003g0247a0001c0002t0001g0245a0001c0003t0003g0246others(13): Show | 16 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.440+104C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189043 | ||||||
| chr11:130189066
|
T | C | 10 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0007t0001g0105others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.440+127T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189066 | ||||||
| chr11:130189087
|
C | T | 11 | a0001c0003t0003g0246a0001c0003t0005g0144a0001c0003t0005g0145others(8): Show | 11 | HG02451.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+148C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189087 | ||||||
| chr11:130189310
|
T | C | 1 | a0010c0029t0001g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.440+371T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189310 | ||||||
| chr11:130189607
|
G | C | 4 | a0001c0001t0001g0237a0001c0002t0001g0239a0001c0023t0001g0236others(1): Show | 4 | HG01074.hp2 HG01884.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-132G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189607 | ||||||
| chr11:130189633
|
A | G | 11 | a0001c0002t0001g0069a0001c0002t0001g0210a0001c0002t0001g0211others(8): Show | 11 | HG00735.hp2 HG01074.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-106A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 4/18 | chr11 | 130189633 | ||||||
| chr11:130189921
|
C | T | 5 | a0001c0019t0003g0208a0004c0030t0001g0190a0006c0014t0001g0147others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+25C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130189921 | ||||||
| chr11:130189979
|
C | T | 1 | a0001c0003t0001g0198 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.598+83C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130189979 | ||||||
| chr11:130190045
|
A | G | 2 | a0001c0002t0002g0010a0001c0002t0002g0159 | 3 | HG01361.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.599-68A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 5/18 | chr11 | 130190045 | ||||||
| chr11:130190216
|
C | A | 1 | a0001c0002t0001g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.634+68C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190216 | ||||||
| chr11:130190262
|
ACGATCTT others(3): Show |
A | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+115_634+124del others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190262 | ||||||
| chr11:130190275
|
G | T | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+127G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190275 | ||||||
| chr11:130190276
|
C | A | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+128C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190276 | ||||||
| chr11:130190277
|
C | T | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+129C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190277 | ||||||
| chr11:130190278
|
C | A | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+130C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190278 | ||||||
| chr11:130190322
|
C | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.635-132C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190322 | ||||||
| chr11:130190344
|
C | T | 9 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-110C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190344 | ||||||
| chr11:130190449
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18992.hp1 | splice_region_variant&intron_variant | LOW | c.635-5C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 6/18 | chr11 | 130190449 | ||||||
| chr11:130190706
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0003g0247 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.875+12G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130190706 | ||||||
| chr11:130190717
|
A | G | 244 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.875+23A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130190717 | ||||||
| chr11:130191121
|
C | T | 8 | a0001c0019t0003g0208a0005c0009t0003g0205a0005c0009t0003g0206others(5): Show | 8 | HG01261.hp2 HG02257.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+427C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191121 | ||||||
| chr11:130191136
|
A | C | 1 | a0001c0028t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.875+442A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191136 | ||||||
| chr11:130191158
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.875+464C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191158 | ||||||
| chr11:130191163
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0003g0247 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.875+469C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191163 | ||||||
| chr11:130191244
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.875+550G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191244 | ||||||
| chr11:130191264
|
C | T | 1 | a0001c0016t0002g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.875+570C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191264 | ||||||
| chr11:130191399
|
C | G | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.875+705C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191399 | ||||||
| chr11:130191452
|
G | A | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+758G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191452 | ||||||
| chr11:130191460
|
C | A | 179 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(176): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.875+766C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191460 | ||||||
| chr11:130191460
|
C | T | 2 | a0002c0006t0001g0225a0002c0006t0001g0229 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.875+766C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191460 | ||||||
| chr11:130191475
|
C | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(18): Show | 22 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.875+781C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191475 | ||||||
| chr11:130191516
|
C | G | 1 | a0001c0016t0002g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.875+822C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191516 | ||||||
| chr11:130191518
|
T | C | 2 | a0001c0002t0001g0210a0001c0002t0001g0211 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.875+824T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191518 | ||||||
| chr11:130191550
|
T | C | 1 | a0001c0001t0003g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.875+856T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191550 | ||||||
| chr11:130191582
|
C | T | 2 | a0001c0023t0001g0236a0001c0035t0001g0158 | 2 | HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.875+888C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191582 | ||||||
| chr11:130191668
|
C | T | 6 | a0001c0003t0001g0219a0001c0007t0001g0191a0001c0007t0001g0192others(3): Show | 6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+974C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191668 | ||||||
| chr11:130191669
|
A | G | 6 | a0001c0003t0001g0219a0001c0007t0001g0191a0001c0007t0001g0192others(3): Show | 6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+975A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191669 | ||||||
| chr11:130191672
|
AGAG | A | 6 | a0001c0003t0001g0219a0001c0007t0001g0191a0001c0007t0001g0192others(3): Show | 6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+979_875+981del others(3): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191672 | ||||||
| chr11:130191676
|
C | A | 6 | a0001c0003t0001g0219a0001c0007t0001g0191a0001c0007t0001g0192others(3): Show | 6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+982C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191676 | ||||||
| chr11:130191689
|
C | CAA | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+1015_875+1016d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | |||||
| chr11:130191689
|
CA | C | 69 | a0001c0001t0001g0233a0001c0001t0001g0269a0001c0001t0001g0276others(66): Show | 69 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.875+1016delA | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | |||||
| chr11:130191689
|
CAA | C | 51 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(48): Show | 53 | HG00140.hp2 HG00323.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.875+1015_875+1016d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | |||||
| chr11:130191689
|
CAAA | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.875+1014_875+1016d others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | |||||
| chr11:130191689
|
CAAAA | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0043a0001c0001t0002g0046others(4): Show | 8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+1013_875+1016d others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130191689 | |||||
| chr11:130191778
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.875+1084T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191778 | ||||||
| chr11:130191852
|
G | A | 4 | a0007c0022t0001g0073a0007c0034t0001g0203a0008c0015t0004g0232others(1): Show | 4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+1158G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191852 | ||||||
| chr11:130191868
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.875+1174C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191868 | ||||||
| chr11:130191892
|
G | A | 233 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.875+1198G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191892 | ||||||
| chr11:130191918
|
G | A | 1 | a0012c0024t0001g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.875+1224G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130191918 | ||||||
| chr11:130192069
|
G | A | 1 | a0001c0003t0005g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.875+1375G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192069 | ||||||
| chr11:130192224
|
C | T | 254 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(251): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.875+1530C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192224 | ||||||
| chr11:130192240
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.875+1546G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192240 | ||||||
| chr11:130192302
|
A | G | 2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.875+1608A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192302 | ||||||
| chr11:130192402
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.875+1708T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192402 | ||||||
| chr11:130192465
|
C | T | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.876-1684C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192465 | ||||||
| chr11:130192492
|
G | A | 1 | a0001c0002t0001g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.876-1657G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192492 | ||||||
| chr11:130192514
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.876-1635G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192514 | ||||||
| chr11:130192588
|
T | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.876-1561T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192588 | ||||||
| chr11:130192631
|
A | G | 1 | a0001c0002t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.876-1518A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192631 | ||||||
| chr11:130192806
|
G | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.876-1343G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192806 | ||||||
| chr11:130192875
|
C | A | 1 | a0004c0008t0004g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.876-1274C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192875 | ||||||
| chr11:130192898
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.876-1251G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130192898 | ||||||
| chr11:130193103
|
G | GT | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.876-1035dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193103 | |||||
| chr11:130193103
|
G | GTT | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0002others(2): Show | 6 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-1036_876-1035d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193103 | |||||
| chr11:130193232
|
C | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.876-917C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193232 | ||||||
| chr11:130193245
|
G | A | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-904G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193245 | ||||||
| chr11:130193338
|
A | G | 1 | a0001c0003t0001g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.876-811A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193338 | ||||||
| chr11:130193357
|
C | T | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.876-792C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193357 | ||||||
| chr11:130193366
|
G | A | 74 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0044others(71): Show | 75 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.876-783G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193366 | ||||||
| chr11:130193476
|
C | CT | 57 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0044others(54): Show | 58 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.876-660dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193476 | |||||
| chr11:130193490
|
C | G | 12 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(9): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-659C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193490 | ||||||
| chr11:130193601
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-548C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193601 | ||||||
| chr11:130193626
|
T | C | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.876-523T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193626 | ||||||
| chr11:130193643
|
T | C | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.876-506T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193643 | ||||||
| chr11:130193684
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.876-465G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193684 | ||||||
| chr11:130193754
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.876-395G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193754 | ||||||
| chr11:130193762
|
G | T | 2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.876-387G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193762 | ||||||
| chr11:130193782
|
T | TTGATTGT others(85): Show |
12 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(9): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-266_876-175dup others(92): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | |||||
| chr11:130193782
|
T | TTGATTGT others(131): Show |
77 | a0001c0001t0001g0012a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 79 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.876-312_876-175dup others(138): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | |||||
| chr11:130193782
|
T | TTGATTGT others(177): Show |
156 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.876-358_876-175dup others(184): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | |||||
| chr11:130193782
|
T | TTGATTGT others(223): Show |
1 | a0001c0001t0003g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-175_876-174ins others(230): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | |||||
| chr11:130193782
|
TTGATTGT others(39): Show |
T | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-220_876-175del others(46): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193782 | |||||
| chr11:130193838
|
C | CAAAGGTG others(39): Show |
2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.876-266_876-265ins others(46): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 130193838 | |||||
| chr11:130193863
|
G | A | 1 | a0001c0007t0001g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.876-286G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130193863 | ||||||
| chr11:130194144
|
C | G | 1 | a0001c0002t0001g0249 | 1 | NA18967.hp2 | splice_region_variant&intron_variant | LOW | c.876-5C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 7/18 | chr11 | 130194144 | ||||||
| chr11:130194328
|
A | G | 259 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1015+40A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194328 | ||||||
| chr11:130194486
|
G | A | 1 | a0001c0003t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1016-154G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194486 | ||||||
| chr11:130194559
|
C | A | 1 | a0001c0003t0001g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1016-81C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 8/18 | chr11 | 130194559 | ||||||
| chr11:130194752
|
G | A | 231 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(228): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1113+15G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194752 | ||||||
| chr11:130194804
|
CTGTGCAG others(3): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1113+72_1113+81del others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194804 | |||||
| chr11:130194809
|
C | T | 2 | a0001c0002t0002g0261a0001c0002t0002g0273 | 2 | HG04115.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1113+72C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194809 | ||||||
| chr11:130194810
|
A | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(259): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1113+73A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194810 | ||||||
| chr11:130194851
|
C | CAT | 12 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(9): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+115_1113+116d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194851 | |||||
| chr11:130194851
|
C | CGT | 13 | a0001c0002t0001g0239a0001c0003t0001g0041a0001c0003t0001g0066others(10): Show | 13 | HG01109.hp2 HG01517.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+114_1113+115i others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194851 | ||||||
| chr11:130194852
|
A | G | 70 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0044others(67): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1113+115A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194852 | ||||||
| chr11:130194852
|
ATG | A | 5 | a0001c0019t0003g0208a0007c0022t0001g0073a0007c0034t0001g0203others(2): Show | 5 | HG02257.hp1 HG03041.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+138_1113+139d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | |||||
| chr11:130194852
|
ATGTG | A | 7 | a0001c0001t0001g0237a0005c0009t0002g0220a0005c0009t0002g0223others(4): Show | 7 | HG01261.hp2 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+136_1113+139d others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | |||||
| chr11:130194852
|
ATGTGTGT others(1): Show |
A | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1113+132_1113+139d others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130194852 | |||||
| chr11:130194875
|
T | C | 3 | a0001c0003t0001g0013a0001c0003t0001g0198a0001c0003t0001g0267 | 3 | HG00642.hp1 HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1113+138T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130194875 | ||||||
| chr11:130195079
|
C | T | 233 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1113+342C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195079 | ||||||
| chr11:130195466
|
G | A | 4 | a0007c0022t0001g0073a0007c0034t0001g0203a0008c0015t0004g0232others(1): Show | 4 | HG02257.hp1 HG03654.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+729G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195466 | ||||||
| chr11:130195542
|
C | T | 2 | a0001c0003t0001g0013a0001c0003t0001g0198 | 2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1114-797C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195542 | ||||||
| chr11:130195581
|
G | T | 2 | a0001c0003t0001g0013a0001c0003t0001g0198 | 2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1114-758G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195581 | ||||||
| chr11:130195637
|
G | A | 245 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(242): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1114-702G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195637 | ||||||
| chr11:130195721
|
C | T | 1 | a0001c0002t0001g0263 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1114-618C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195721 | ||||||
| chr11:130195777
|
C | T | 6 | a0005c0009t0002g0220a0005c0009t0002g0223a0005c0009t0003g0205others(3): Show | 6 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-562C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195777 | ||||||
| chr11:130195801
|
T | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1114-538T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195801 | ||||||
| chr11:130195802
|
G | A | 1 | a0001c0001t0003g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1114-537G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195802 | ||||||
| chr11:130195843
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0070 | 2 | NA18964.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1114-496A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195843 | ||||||
| chr11:130195851
|
TCA | T | 230 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1114-487_1114-486d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195851 | ||||||
| chr11:130195852
|
CAA | C | 12 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(9): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1114-473_1114-472d others(4): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130195852 | |||||
| chr11:130195871
|
A | T | 4 | a0001c0003t0003g0246a0001c0003t0005g0144a0001c0003t0005g0145others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-468A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195871 | ||||||
| chr11:130195876
|
G | T | 245 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(242): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1114-463G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195876 | ||||||
| chr11:130195893
|
G | C | 1 | a0001c0001t0002g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1114-446G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195893 | ||||||
| chr11:130195928
|
G | A | 9 | a0001c0001t0001g0237a0001c0023t0001g0236a0001c0035t0001g0158others(6): Show | 9 | HG01074.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-411G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130195928 | ||||||
| chr11:130196194
|
C | A | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1114-145C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130196194 | ||||||
| chr11:130196194
|
C | CAAAA | 13 | a0001c0001t0002g0030a0004c0008t0001g0162a0004c0008t0001g0174others(10): Show | 13 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1114-144_1114-143i others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 130196194 | |||||
| chr11:130196273
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 18 | HG00408.hp1 HG02559.hp2 HG03540.hp1 others(15): Show |
intron_variant | MODIFIER | c.1114-66T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 9/18 | chr11 | 130196273 | ||||||
| chr11:130196477
|
G | A | 255 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(252): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1223+29G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196477 | ||||||
| chr11:130196523
|
C | T | 11 | a0001c0001t0001g0237a0001c0001t0004g0199a0001c0001t0004g0200others(8): Show | 11 | HG01074.hp2 HG01261.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1224-47C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196523 | ||||||
| chr11:130196557
|
G | GC | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
splice_region_variant&intron_variant | LOW | c.1224-6dupC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr11 | 130196557 | |||||
| chr11:130196565
|
T | C | 7 | a0003c0005t0001g0005a0003c0005t0001g0024a0003c0005t0001g0082others(4): Show | 7 | HG00639.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1224-5T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 10/18 | chr11 | 130196565 | ||||||
| chr11:130196893
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0064 | 3 | HG01069.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1354+193C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196893 | ||||||
| chr11:130196972
|
T | C | 233 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1354+272T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196972 | ||||||
| chr11:130196976
|
C | T | 233 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1354+276C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130196976 | ||||||
| chr11:130197005
|
C | T | 134 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1354+305C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197005 | ||||||
| chr11:130197007
|
G | A | 233 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1354+307G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197007 | ||||||
| chr11:130197062
|
C | T | 232 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1354+362C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197062 | ||||||
| chr11:130197174
|
G | C | 223 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(220): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1354+474G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197174 | ||||||
| chr11:130197288
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1355-553C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197288 | ||||||
| chr11:130197331
|
G | A | 210 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1355-510G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197331 | ||||||
| chr11:130197663
|
G | A | 1 | a0004c0008t0004g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1355-178G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 11/18 | chr11 | 130197663 | ||||||
| chr11:130197982
|
C | T | 14 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0002g0030others(11): Show | 14 | HG00621.hp2 HG00639.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1459+37C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130197982 | ||||||
| chr11:130197997
|
C | T | 91 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(88): Show | 93 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1459+52C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130197997 | ||||||
| chr11:130198026
|
C | T | 2 | a0005c0009t0003g0206a0005c0009t0003g0207 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1459+81C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198026 | ||||||
| chr11:130198092
|
A | C | 88 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(85): Show | 90 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1459+147A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198092 | ||||||
| chr11:130198110
|
T | C | 1 | a0002c0004t0002g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1459+165T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198110 | ||||||
| chr11:130198119
|
T | TATGGCAG others(1): Show |
4 | a0001c0003t0003g0246a0001c0003t0005g0144a0001c0003t0005g0145others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+174_1459+175i others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198119 | ||||||
| chr11:130198120
|
G | T | 4 | a0001c0003t0003g0246a0001c0003t0005g0144a0001c0003t0005g0145others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+175G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 12/18 | chr11 | 130198120 | ||||||
| chr11:130198465
|
A | G | 3 | a0001c0002t0003g0053a0006c0014t0001g0147a0006c0014t0001g0256 | 3 | HG01255.hp1 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1571-43A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/18 | chr11 | 130198465 | ||||||
| chr11:130198470
|
C | T | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1571-38C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 13/18 | chr11 | 130198470 | ||||||
| chr11:130198628
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0002g0034a0001c0001t0002g0085 | 3 | HG00621.hp1 HG02074.hp2 NA19074.hp1 |
splice_region_variant&intron_variant | LOW | c.1684+7C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198628 | ||||||
| chr11:130198659
|
C | T | 135 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1684+38C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198659 | ||||||
| chr11:130198688
|
C | T | 3 | a0001c0001t0002g0062a0007c0034t0001g0203a0011c0021t0002g0035 | 3 | HG03017.hp2 HG04199.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1684+67C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 14/18 | chr11 | 130198688 | ||||||
| chr11:130199153
|
C | T | 1 | a0001c0003t0005g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1807+84C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199153 | ||||||
| chr11:130199250
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1807+181C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199250 | ||||||
| chr11:130199291
|
A | G | 17 | a0001c0003t0001g0013a0001c0003t0001g0041a0001c0003t0001g0170others(14): Show | 17 | HG01099.hp1 HG01517.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1807+222A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199291 | ||||||
| chr11:130199299
|
G | A | 1 | a0001c0019t0003g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1807+230G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199299 | ||||||
| chr11:130199623
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1808-328A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199623 | ||||||
| chr11:130199661
|
G | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1808-290G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199661 | ||||||
| chr11:130199679
|
G | A | 3 | a0001c0002t0001g0239a0004c0008t0001g0162a0004c0008t0001g0174 | 3 | HG01884.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1808-272G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199679 | ||||||
| chr11:130199743
|
G | A | 3 | a0001c0001t0002g0071a0001c0001t0002g0113a0001c0001t0002g0130 | 3 | HG00140.hp1 HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1808-208G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199743 | ||||||
| chr11:130199775
|
T | C | 10 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1808-176T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199775 | ||||||
| chr11:130199809
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1808-142C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199809 | ||||||
| chr11:130199865
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1808-86G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199865 | ||||||
| chr11:130199895
|
T | G | 282 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(279): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1808-56T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 15/18 | chr11 | 130199895 | ||||||
| chr11:130200298
|
T | C | 2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1994+161T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200298 | ||||||
| chr11:130200350
|
G | A | 2 | a0006c0014t0001g0147a0006c0014t0001g0256 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1994+213G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200350 | ||||||
| chr11:130200560
|
C | A | 1 | a0001c0002t0001g0249 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1994+423C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200560 | ||||||
| chr11:130200637
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+500C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200637 | ||||||
| chr11:130200649
|
G | A | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(150): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1994+512G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200649 | ||||||
| chr11:130200905
|
C | T | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1994+768C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130200905 | ||||||
| chr11:130201004
|
A | G | 35 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(32): Show | 36 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1994+867A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201004 | ||||||
| chr11:130201133
|
A | G | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1994+996A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201133 | ||||||
| chr11:130201189
|
C | T | 2 | a0004c0008t0001g0162a0004c0008t0001g0174 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1994+1052C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201189 | ||||||
| chr11:130201290
|
A | G | 13 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(10): Show | 13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1153A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201290 | ||||||
| chr11:130201298
|
A | G | 13 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(10): Show | 13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1161A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201298 | ||||||
| chr11:130201324
|
C | T | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1187C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201324 | ||||||
| chr11:130201358
|
G | T | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1221G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201358 | ||||||
| chr11:130201398
|
G | A | 13 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(10): Show | 13 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1994+1261G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201398 | ||||||
| chr11:130201442
|
G | T | 8 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(5): Show | 8 | HG01109.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1994+1305G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201442 | ||||||
| chr11:130201450
|
G | A | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1313G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201450 | ||||||
| chr11:130201704
|
T | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0023others(147): Show | 156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1994+1567T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201704 | ||||||
| chr11:130201795
|
C | T | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1994+1658C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201795 | ||||||
| chr11:130201925
|
C | A | 1 | a0002c0006t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1994+1788C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130201925 | ||||||
| chr11:130202074
|
T | G | 3 | a0001c0003t0001g0013a0001c0003t0001g0066a0001c0003t0001g0198 | 3 | HG00735.hp1 HG01109.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1994+1937T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202074 | ||||||
| chr11:130202198
|
G | A | 6 | a0004c0008t0001g0162a0004c0008t0001g0174a0004c0008t0004g0171others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1994+2061G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202198 | ||||||
| chr11:130202203
|
G | A | 2 | a0001c0001t0001g0068a0001c0003t0001g0041 | 2 | HG01517.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1994+2066G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202203 | ||||||
| chr11:130202462
|
T | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1994+2325T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202462 | ||||||
| chr11:130202489
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(31): Show | 35 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1994+2352G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202489 | ||||||
| chr11:130202631
|
A | G | 5 | a0001c0002t0003g0053a0001c0003t0001g0013a0001c0003t0001g0041others(2): Show | 5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1994+2494A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202631 | ||||||
| chr11:130202674
|
C | T | 7 | a0002c0006t0001g0229a0004c0008t0001g0162a0004c0008t0001g0174others(4): Show | 7 | HG01891.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1994+2537C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202674 | ||||||
| chr11:130202685
|
T | C | 199 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(196): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1994+2548T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202685 | ||||||
| chr11:130202702
|
C | T | 1 | a0003c0005t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1994+2565C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202702 | ||||||
| chr11:130202715
|
C | A | 1 | a0001c0003t0005g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1994+2578C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202715 | ||||||
| chr11:130202739
|
G | A | 14 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(11): Show | 14 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1994+2602G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202739 | ||||||
| chr11:130202836
|
A | G | 18 | a0001c0002t0003g0053a0001c0003t0001g0013a0001c0003t0001g0041others(15): Show | 18 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1994+2699A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202836 | ||||||
| chr11:130202888
|
G | C | 18 | a0001c0002t0003g0053a0001c0003t0001g0013a0001c0003t0001g0041others(15): Show | 18 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1994+2751G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130202888 | ||||||
| chr11:130203023
|
A | G | 14 | a0001c0002t0001g0239a0001c0003t0001g0170a0001c0007t0001g0105others(11): Show | 14 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1994+2886A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203023 | ||||||
| chr11:130203171
|
C | T | 5 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0041others(2): Show | 5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1994+3034C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203171 | ||||||
| chr11:130203446
|
C | T | 1 | a0001c0002t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1994+3309C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203446 | ||||||
| chr11:130203460
|
C | T | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3323C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203460 | ||||||
| chr11:130203638
|
A | G | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3501A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203638 | ||||||
| chr11:130203643
|
T | C | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3506T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203643 | ||||||
| chr11:130203647
|
T | C | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3510T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203647 | ||||||
| chr11:130203675
|
C | T | 2 | a0001c0003t0001g0176a0001c0003t0001g0267 | 2 | HG00642.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1994+3538C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203675 | ||||||
| chr11:130203735
|
C | T | 4 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(1): Show | 4 | HG01255.hp1 HG01517.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994+3598C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203735 | ||||||
| chr11:130203770
|
A | G | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+3633A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203770 | ||||||
| chr11:130203809
|
T | C | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3672T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203809 | ||||||
| chr11:130203819
|
A | G | 1 | a0002c0006t0001g0217 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1994+3682A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203819 | ||||||
| chr11:130203842
|
C | T | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3705C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203842 | ||||||
| chr11:130203843
|
G | A | 3 | a0003c0005t0001g0124a0003c0005t0001g0125a0003c0005t0002g0022 | 3 | HG01934.hp2 HG01952.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1994+3706G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203843 | ||||||
| chr11:130203887
|
C | T | 1 | a0001c0001t0002g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1994+3750C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203887 | ||||||
| chr11:130203888
|
G | A | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1994+3751G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203888 | ||||||
| chr11:130203953
|
C | A | 8 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(5): Show | 8 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1994+3816C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130203953 | ||||||
| chr11:130204018
|
C | T | 8 | a0001c0001t0001g0280a0001c0002t0001g0210a0001c0002t0001g0211others(5): Show | 8 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1994+3881C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204018 | ||||||
| chr11:130204121
|
G | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1994+3984G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204121 | ||||||
| chr11:130204182
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1994+4045T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204182 | ||||||
| chr11:130204242
|
G | A | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1994+4105G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204242 | ||||||
| chr11:130204295
|
A | G | 182 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(179): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1995-4115A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204295 | ||||||
| chr11:130204376
|
C | A | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-4034C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204376 | ||||||
| chr11:130204433
|
A | C | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3977A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204433 | ||||||
| chr11:130204497
|
G | T | 4 | a0001c0003t0003g0246a0001c0003t0005g0144a0001c0003t0005g0145others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-3913G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204497 | ||||||
| chr11:130204540
|
G | A | 5 | a0001c0001t0001g0280a0001c0003t0001g0013a0001c0003t0001g0041others(2): Show | 5 | HG00735.hp1 HG01109.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995-3870G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204540 | ||||||
| chr11:130204587
|
A | G | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3823A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204587 | ||||||
| chr11:130204599
|
G | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1995-3811G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204599 | ||||||
| chr11:130204685
|
A | T | 1 | a0001c0003t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1995-3725A>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204685 | ||||||
| chr11:130204704
|
T | TA | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3706_1995-370 others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130204704 | ||||||
| chr11:130205043
|
T | C | 5 | a0001c0001t0001g0233a0001c0003t0003g0246a0001c0003t0005g0144others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995-3367T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205043 | ||||||
| chr11:130205108
|
T | C | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-3302T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205108 | ||||||
| chr11:130205159
|
A | G | 187 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(184): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1995-3251A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205159 | ||||||
| chr11:130205370
|
C | A | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3040C>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205370 | ||||||
| chr11:130205372
|
C | G | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3038C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205372 | ||||||
| chr11:130205374
|
T | C | 182 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(179): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1995-3036T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205374 | ||||||
| chr11:130205375
|
G | A | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3035G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205375 | ||||||
| chr11:130205377
|
C | G | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3033C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205377 | ||||||
| chr11:130205378
|
T | A | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3032T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205378 | ||||||
| chr11:130205379
|
T | C | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3031T>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205379 | ||||||
| chr11:130205381
|
G | A | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3029G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205381 | ||||||
| chr11:130205382
|
C | T | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3028C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205382 | ||||||
| chr11:130205383
|
C | G | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3027C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205383 | ||||||
| chr11:130205386
|
C | T | 1 | a0003c0005t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995-3024C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205386 | ||||||
| chr11:130205481
|
C | T | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-2929C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205481 | ||||||
| chr11:130205537
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0055others(19): Show | 24 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1995-2873G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205537 | ||||||
| chr11:130205539
|
G | A | 161 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(158): Show | 166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1995-2871G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205539 | ||||||
| chr11:130205653
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1995-2757C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205653 | ||||||
| chr11:130205666
|
C | T | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-2744C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205666 | ||||||
| chr11:130205680
|
A | G | 127 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0095others(124): Show | 131 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1995-2730A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205680 | ||||||
| chr11:130205683
|
A | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0278 | 2 | NA18971.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1995-2727A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205683 | ||||||
| chr11:130205699
|
G | GT | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0055others(41): Show | 46 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1995-2700dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130205699 | |||||
| chr11:130205699
|
G | GTT | 10 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0110others(7): Show | 10 | HG00438.hp2 HG00642.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1995-2701_1995-270 others(6): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130205699 | |||||
| chr11:130205706
|
T | G | 2 | a0005c0009t0002g0220a0005c0009t0002g0223 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1995-2704T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205706 | ||||||
| chr11:130205709
|
T | G | 1 | a0001c0019t0003g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1995-2701T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205709 | ||||||
| chr11:130205710
|
T | G | 1 | a0001c0031t0007g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1995-2700T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205710 | ||||||
| chr11:130205710
|
TG | T | 97 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0059others(94): Show | 102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1995-2699delG | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205710 | ||||||
| chr11:130205711
|
G | T | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 186 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1995-2699G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205711 | ||||||
| chr11:130205728
|
G | A | 6 | a0001c0001t0001g0280a0001c0001t0002g0032a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1995-2682G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205728 | ||||||
| chr11:130205741
|
C | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(202): Show | 212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1995-2669C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205741 | ||||||
| chr11:130205829
|
G | A | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2581G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205829 | ||||||
| chr11:130205855
|
C | T | 35 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(32): Show | 36 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1995-2555C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205855 | ||||||
| chr11:130205857
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1995-2553C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205857 | ||||||
| chr11:130205888
|
G | A | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2522G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205888 | ||||||
| chr11:130205965
|
A | G | 9 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(6): Show | 9 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1995-2445A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205965 | ||||||
| chr11:130205972
|
C | T | 3 | a0001c0001t0001g0237a0001c0023t0001g0236a0001c0035t0001g0158 | 3 | HG01074.hp2 HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1995-2438C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130205972 | ||||||
| chr11:130206120
|
G | T | 1 | a0005c0009t0003g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1995-2290G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206120 | ||||||
| chr11:130206230
|
C | T | 1 | a0001c0003t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1995-2180C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206230 | ||||||
| chr11:130206231
|
G | A | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0004c0008t0004g0241others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1995-2179G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206231 | ||||||
| chr11:130206237
|
G | A | 7 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(4): Show | 7 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995-2173G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206237 | ||||||
| chr11:130206311
|
G | A | 11 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0004t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995-2099G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206311 | ||||||
| chr11:130206390
|
A | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0057others(2): Show | 7 | HG00408.hp1 HG02080.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995-2020A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206390 | ||||||
| chr11:130206395
|
C | T | 1 | a0003c0005t0001g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1995-2015C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206395 | ||||||
| chr11:130206395
|
CGTGA | C | 117 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0149others(114): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-2011_1995-200 others(8): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206395 | |||||
| chr11:130206439
|
C | T | 117 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0149others(114): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-1971C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206439 | ||||||
| chr11:130206443
|
C | T | 1 | a0001c0003t0001g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1995-1967C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206443 | ||||||
| chr11:130206460
|
T | TG | 6 | a0001c0001t0001g0280a0001c0002t0003g0053a0001c0003t0001g0013others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995-1950_1995-194 others(5): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206460 | ||||||
| chr11:130206567
|
C | CT | 152 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0149others(149): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1995-1832dupT | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206567 | |||||
| chr11:130206648
|
AC | A | 117 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0149others(114): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1995-1760delC | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130206648 | |||||
| chr11:130206757
|
G | A | 2 | a0008c0015t0004g0232a0008c0015t0004g0234 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1995-1653G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206757 | ||||||
| chr11:130206766
|
C | T | 1 | a0001c0002t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1995-1644C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206766 | ||||||
| chr11:130206807
|
A | G | 1 | a0001c0002t0001g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1995-1603A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206807 | ||||||
| chr11:130206887
|
T | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0055others(9): Show | 14 | HG00408.hp1 HG02080.hp2 HG03831.hp1 others(11): Show |
intron_variant | MODIFIER | c.1995-1523T>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206887 | ||||||
| chr11:130206999
|
G | A | 29 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0042others(26): Show | 31 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1995-1411G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130206999 | ||||||
| chr11:130207063
|
G | A | 12 | a0001c0001t0004g0199a0001c0001t0004g0200a0002c0006t0001g0215others(9): Show | 12 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1995-1347G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207063 | ||||||
| chr11:130207065
|
A | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0263 | 2 | HG02040.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1995-1345A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207065 | ||||||
| chr11:130207071
|
G | A | 10 | a0001c0003t0001g0170a0001c0007t0001g0105a0002c0006t0001g0214others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1995-1339G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207071 | ||||||
| chr11:130207128
|
C | T | 207 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(204): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1995-1282C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207128 | ||||||
| chr11:130207231
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1995-1179C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207231 | ||||||
| chr11:130207372
|
G | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0055others(14): Show | 19 | HG00408.hp1 HG00642.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1995-1038G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207372 | ||||||
| chr11:130207615
|
C | G | 1 | a0013c0032t0002g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1995-795C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207615 | ||||||
| chr11:130207760
|
G | C | 2 | a0001c0003t0001g0176a0001c0003t0001g0267 | 2 | HG00642.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1995-650G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207760 | ||||||
| chr11:130207899
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0055others(23): Show | 28 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1995-511C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207899 | ||||||
| chr11:130207945
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0002g0114 | 2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1995-465C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130207945 | ||||||
| chr11:130208020
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1995-390G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208020 | ||||||
| chr11:130208073
|
CAATAAAT others(1): Show |
C | 28 | a0001c0001t0001g0156a0001c0001t0002g0004a0001c0001t0002g0021others(25): Show | 30 | HG00735.hp2 HG01069.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1995-321_1995-314d others(10): Show |
ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 130208073 | |||||
| chr11:130208194
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1995-216G>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208194 | ||||||
| chr11:130208281
|
G | A | 7 | a0002c0006t0001g0214a0002c0006t0001g0216a0002c0006t0001g0217others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995-129G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208281 | ||||||
| chr11:130208372
|
G | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1995-38G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 16/18 | chr11 | 130208372 | ||||||
| chr11:130208850
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2269+166A>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208850 | ||||||
| chr11:130208894
|
C | T | 1 | a0001c0003t0001g0087 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2269+210C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208894 | ||||||
| chr11:130208899
|
C | G | 1 | a0001c0002t0001g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2269+215C>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130208899 | ||||||
| chr11:130209115
|
A | C | 1 | a0001c0001t0002g0079 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2270-327A>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209115 | ||||||
| chr11:130209199
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0023t0001g0236 | 3 | HG01074.hp2 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2270-243C>T | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209199 | ||||||
| chr11:130209215
|
G | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2270-227G>A | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209215 | ||||||
| chr11:130209320
|
T | G | 21 | a0001c0001t0001g0156a0001c0003t0001g0029a0001c0003t0001g0170others(18): Show | 21 | HG01069.hp1 HG01099.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2270-122T>G | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209320 | ||||||
| chr11:130209339
|
G | C | 125 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0269others(122): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2270-103G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 17/18 | chr11 | 130209339 | ||||||
| chr11:130209582
|
G | C | 1 | a0001c0002t0001g0239 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.2406+4G>C | ST14 | ENSG00000149418.11 | transcript | ENST00000278742.6 | protein_coding | 18/18 | chr11 | 130209582 |