Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56946 |
|---|---|
| ensemblid | ENSG00000158636.17 |
| hgncid | 18071 |
| symbol | EMSY |
| name | EMSY transcriptional repressor, BRCA2 interacting |
| refseq_nuc | NM_001300942.2 |
| refseq_prot | NP_001287871.1 |
| ensembl_nuc | ENST00000695367.1 |
| ensembl_prot | ENSP00000511840.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 76445018 |
| end | 76553031 |
| strand | + |
| ver | v1.2 |
| region | chr11:76445018-76553031 |
| region5000 | chr11:76440018-76558031 |
| regionname0 | EMSY_chr11_76445018_76553031 |
| regionname5000 | EMSY_chr11_76440018_76558031 |
| 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 | 1337 | 354 | 78 | 64 | 156 | 16 | 38 | 122 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0002 | 0/0 | 1337 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0003 | 0/0 | 1337 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0004 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4014 | 275 | 57 | 45 | 132 | 11 | 28 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0002 | 0/0 | 4014 | 71 | 16 | 16 | 24 | 5 | 10 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0003 | 0/0 | 4014 | 4 | 4 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0004 | 0/0 | 4014 | 4 | 1 | 3 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0005 | 0/0 | 4014 | 3 | 0 | 0 | 3 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0006 | 0/0 | 4014 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| c0007 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| 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 | 1/0 | 3036 | 132 | 43 | 16 | 56 | 8 | 8 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0002 | 0/1 | 3037 | 121 | 17 | 20 | 64 | 4 | 15 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0003 | 0/0 | 3037 | 51 | 4 | 15 | 20 | 3 | 9 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0004 | 0/0 | 3036 | 10 | 0 | 0 | 9 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0005 | 0/0 | 3037 | 5 | 0 | 0 | 5 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0006 | 0/0 | 3036 | 5 | 5 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0007 | 0/0 | 3037 | 5 | 0 | 5 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0008 | 0/0 | 3037 | 3 | 0 | 0 | 3 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0009 | 0/0 | 3037 | 3 | 0 | 3 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0010 | 0/0 | 3036 | 3 | 0 | 1 | 0 | 0 | 2 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0011 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0012 | 0/0 | 3037 | 2 | 0 | 1 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0013 | 0/0 | 3037 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0014 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0015 | 0/0 | 3037 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0016 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0017 | 0/0 | 3037 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0018 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0019 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0020 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0021 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0022 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0023 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0024 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0025 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0026 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| t0027 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0290 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4014 | 275 | 57 | 45 | 132 | 11 | 28 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002 | 0/0 | 4014 | 71 | 16 | 16 | 24 | 5 | 10 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0003 | 0/0 | 4014 | 4 | 4 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0004 | 0/0 | 4014 | 4 | 1 | 3 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0002c0005 | 0/0 | 4014 | 3 | 0 | 0 | 3 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0003c0006 | 0/0 | 4014 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0004c0007 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7049 | 62 | 21 | 2 | 33 | 3 | 2 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0002 | 0/1 | 7050 | 120 | 17 | 20 | 63 | 4 | 15 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0003 | 0/0 | 7050 | 45 | 3 | 13 | 17 | 3 | 9 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0004 | 0/0 | 7049 | 10 | 0 | 0 | 9 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0005 | 0/0 | 7050 | 5 | 0 | 0 | 5 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0006 | 0/0 | 7049 | 5 | 5 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0007 | 0/0 | 7050 | 5 | 0 | 5 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0008 | 0/0 | 7050 | 3 | 0 | 0 | 3 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0009 | 0/0 | 7050 | 3 | 0 | 3 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0011 | 0/0 | 7049 | 3 | 3 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0012 | 0/0 | 7050 | 2 | 0 | 1 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0013 | 0/0 | 7050 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0014 | 0/0 | 7049 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0015 | 0/0 | 7050 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0016 | 0/0 | 7049 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0018 | 0/0 | 7050 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0019 | 0/0 | 7050 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0020 | 0/0 | 7050 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0025 | 0/0 | 7049 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0026 | 0/0 | 7049 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0001t0027 | 0/0 | 7049 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0001 | 0/0 | 7049 | 64 | 16 | 14 | 23 | 5 | 6 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0010 | 0/0 | 7049 | 3 | 0 | 1 | 0 | 0 | 2 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0021 | 0/0 | 7049 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0022 | 0/0 | 7049 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0023 | 0/0 | 7049 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0002t0024 | 0/0 | 7049 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0003t0001 | 0/0 | 7049 | 4 | 4 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0004t0003 | 0/0 | 7050 | 3 | 1 | 2 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0001c0004t0017 | 0/0 | 7050 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0002c0005t0003 | 0/0 | 7050 | 3 | 0 | 0 | 3 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0003c0006t0001 | 0/0 | 7049 | 2 | 2 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| a0004c0007t0002 | 0/0 | 7050 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | copy fasta | chr11 | 76440018 | 76558031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0290 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0009g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0012g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0013g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0014g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0015g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0016g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0019g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0020g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0025g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0026g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0001t0027g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0010g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0010g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0010g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0021g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0022g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0023g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0002t0024g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0004t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0004t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0001c0004t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0002c0005t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0002c0005t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0002c0005t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0003c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0003c0006t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| a0004c0007t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0209 | EUR | GBR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0267 | EUR | GBR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | GBR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | GBR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | FIN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | FIN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0075 | EUR | FIN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0289 | EUR | FIN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00438 | hp2 | a0002 | c0005 | t0003 | g0202 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00621 | hp2 | a0002 | c0005 | t0003 | g0198 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0218 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00642 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | CHS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00741 | hp1 | a0001 | c0002 | t0023 | g0033 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01071 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01099 | hp1 | a0001 | c0001 | t0027 | g0309 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01167 | hp1 | a0001 | c0004 | t0003 | g0199 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01168 | hp2 | a0001 | c0004 | t0017 | g0001 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0130 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0277 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01261 | hp2 | a0001 | c0002 | t0010 | g0034 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0207 | EUR | IBS | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0129 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0128 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0124 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | CDX | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CDX | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CDX | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0247 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0187 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02273 | hp1 | a0001 | c0001 | t0007 | g0126 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0082 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02572 | hp2 | a0003 | c0006 | t0001 | g0250 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0118 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0087 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02698 | hp2 | a0001 | c0002 | t0010 | g0051 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02818 | hp2 | a0003 | c0006 | t0001 | g0249 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0084 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0091 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03098 | hp1 | a0001 | c0001 | t0026 | g0354 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0357 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03225 | hp1 | a0001 | c0001 | t0025 | g0355 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0320 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0288 | AFR | MSL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0248 | AFR | GWD | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03688 | hp2 | a0001 | c0001 | t0012 | g0216 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03710 | hp2 | a0001 | c0002 | t0024 | g0064 | SAS | PJL | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03942 | hp1 | a0001 | c0002 | t0022 | g0022 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04199 | hp2 | a0001 | c0002 | t0010 | g0044 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG04228 | hp2 | a0001 | c0001 | t0015 | g0246 | SAS | STU | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | CHB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0190 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18966 | hp2 | a0002 | c0005 | t0003 | g0197 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18973 | hp1 | a0001 | c0001 | t0019 | g0306 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19004 | hp1 | a0001 | c0002 | t0021 | g0079 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19079 | hp2 | a0004 | c0007 | t0002 | g0121 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19084 | hp2 | a0001 | c0001 | t0020 | g0240 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19089 | hp1 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0287 | AFR | YRI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ASW | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | ASW | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | TSI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | TSI | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | GIH | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | USA | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | USA | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | USA | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | USA | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0094 | AFR | LWK | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0178 | REF | REF | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0290 | REF | REF | EMSY_chr11_76440018_76558031 | EMSY | chr11 | 76440018 | 76558031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76459999
|
G | A | 1 | a0003 | 2 | HG02572.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.530G>A | p.Ser177Asn | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/22 | 680/7049 | 530/4014 | 177/1337 | chr11 | 76459999 | ||
| chr11:76472678
|
A | G | 1 | a0002 | 3 | HG00438.hp2 HG00621.hp2 NA18966.hp2 |
missense_variant | MODERATE | c.991A>G | p.Thr331Ala | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/22 | 1141/7049 | 991/4014 | 331/1337 | chr11 | 76472678 | ||
| chr11:76544410
|
T | G | 1 | a0004 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.2906T>G | p.Leu969Arg | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/22 | 3056/7049 | 2906/4014 | 969/1337 | chr11 | 76544410 | ||
| chr11:76553029
|
G | A | 1 | a0001 | 1 | HG03710.hp2 | splice_region_variant | LOW | c.*2883G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | chr11 | 76553029 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76463865
|
C | A | 1 | a0001c0003 | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.661C>A | p.Arg221Arg | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/22 | 811/7049 | 661/4014 | 221/1337 | chr11 | 76463865 | ||
| chr11:76528450
|
C | G | 1 | a0003c0006 | 2 | HG02572.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.2223C>G | p.Ser741Ser | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/22 | 2373/7049 | 2223/4014 | 741/1337 | chr11 | 76528450 | ||
| chr11:76544771
|
C | G | 1 | a0001c0004 | 4 | HG00642.hp2 HG01167.hp1 HG01168.hp2 others(1): Show |
synonymous_variant | LOW | c.3267C>G | p.Pro1089Pro | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/22 | 3417/7049 | 3267/4014 | 1089/1337 | chr11 | 76544771 | ||
| chr11:76546171
|
T | C | 1 | a0001c0002 | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
synonymous_variant | LOW | c.3693T>C | p.Thr1231Thr | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/22 | 3843/7049 | 3693/4014 | 1231/1337 | chr11 | 76546171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76445038
|
C | T | 1 | a0001c0001t0007 | 5 | HG01175.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/22 | 1901 | chr11 | 76445038 | |||||
| chr11:76445097
|
G | A | 1 | a0001c0001t0015 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/22 | 1842 | chr11 | 76445097 | |||||
| chr11:76550343
|
T | A | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 197 | chr11 | 76550343 | |||||
| chr11:76550360
|
G | GA | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(13): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*223dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 224 | INFO_REALIGN_3_PRIME | chr11 | 76550360 | ||||
| chr11:76550400
|
T | C | 1 | a0001c0002t0021 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 254 | chr11 | 76550400 | |||||
| chr11:76550454
|
A | C | 1 | a0001c0001t0005 | 5 | HG02074.hp2 NA18949.hp2 NA18964.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*308A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 308 | chr11 | 76550454 | |||||
| chr11:76550489
|
A | G | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*343A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 343 | chr11 | 76550489 | |||||
| chr11:76550518
|
T | C | 1 | a0001c0004t0017 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 372 | chr11 | 76550518 | |||||
| chr11:76550570
|
T | G | 1 | a0001c0002t0022 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 424 | chr11 | 76550570 | |||||
| chr11:76550777
|
C | G | 1 | a0001c0001t0009 | 3 | HG01070.hp2 HG01071.hp1 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*631C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 631 | chr11 | 76550777 | |||||
| chr11:76550899
|
G | C | 1 | a0001c0002t0010 | 3 | HG01261.hp2 HG02698.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*753G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 753 | chr11 | 76550899 | |||||
| chr11:76551031
|
T | G | 1 | a0001c0001t0018 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 885 | chr11 | 76551031 | |||||
| chr11:76551084
|
A | G | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(3): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*938A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 938 | chr11 | 76551084 | |||||
| chr11:76551118
|
G | A | 1 | a0001c0001t0014 | 2 | HG03453.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*972G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 972 | chr11 | 76551118 | |||||
| chr11:76551205
|
G | A | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 1059 | chr11 | 76551205 | |||||
| chr11:76551279
|
C | T | 1 | a0001c0001t0027 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1133C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 1133 | chr11 | 76551279 | |||||
| chr11:76551608
|
G | T | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1462G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 1462 | chr11 | 76551608 | |||||
| chr11:76551669
|
C | T | 1 | a0001c0001t0012 | 2 | HG00639.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1523C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 1523 | chr11 | 76551669 | |||||
| chr11:76552113
|
T | C | 1 | a0001c0002t0023 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1967T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 1967 | chr11 | 76552113 | |||||
| chr11:76552182
|
T | C | 1 | a0001c0001t0008 | 3 | NA18959.hp2 NA18970.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2036T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2036 | chr11 | 76552182 | |||||
| chr11:76552289
|
C | T | 1 | a0001c0001t0026 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2143 | chr11 | 76552289 | |||||
| chr11:76552383
|
A | G | 1 | a0001c0001t0026 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2237 | chr11 | 76552383 | |||||
| chr11:76552415
|
C | T | 1 | a0001c0001t0013 | 2 | HG02622.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2269C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2269 | chr11 | 76552415 | |||||
| chr11:76552531
|
A | G | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2385A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2385 | chr11 | 76552531 | |||||
| chr11:76552807
|
C | T | 1 | a0001c0001t0025 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2661C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2661 | chr11 | 76552807 | |||||
| chr11:76552921
|
T | A | 1 | a0001c0001t0006 | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2775T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2775 | chr11 | 76552921 | |||||
| chr11:76552924
|
C | G | 1 | a0001c0001t0004 | 10 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2778C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 22/22 | 2778 | chr11 | 76552924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76445218
|
G | T | 1 | a0001c0001t0002g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-40+90G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445218 | ||||||
| chr11:76445282
|
G | C | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-40+154G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445282 | ||||||
| chr11:76445534
|
T | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG01175.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-40+406T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445534 | ||||||
| chr11:76445535
|
C | G | 35 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(32): Show | 35 | HG00609.hp2 HG01106.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-40+407C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445535 | ||||||
| chr11:76445586
|
C | T | 1 | a0001c0001t0003g0321 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-40+458C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445586 | ||||||
| chr11:76445592
|
T | G | 1 | a0001c0001t0002g0008 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-40+464T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445592 | ||||||
| chr11:76445601
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-40+473C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445601 | ||||||
| chr11:76445744
|
G | A | 33 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(30): Show | 33 | HG00609.hp2 HG01106.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-40+616G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445744 | ||||||
| chr11:76445761
|
C | T | 1 | a0001c0001t0013g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40+633C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445761 | ||||||
| chr11:76445825
|
C | T | 1 | a0001c0001t0002g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-40+697C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445825 | ||||||
| chr11:76445836
|
C | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40+708C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445836 | ||||||
| chr11:76445929
|
G | A | 70 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-40+801G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76445929 | ||||||
| chr11:76446046
|
G | C | 1 | a0001c0001t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-39-854G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446046 | ||||||
| chr11:76446089
|
G | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-39-811G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446089 | ||||||
| chr11:76446240
|
T | A | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-39-660T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446240 | ||||||
| chr11:76446311
|
ATG | A | 262 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(259): Show | 262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-39-577_-39-576del others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446311 | |||||
| chr11:76446313
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-39-587G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446313 | ||||||
| chr11:76446317
|
G | GTGTGTAT others(43): Show |
2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-39-578_-39-577ins others(50): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446317 | |||||
| chr11:76446319
|
G | GTGTATAT others(17): Show |
61 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(58): Show | 62 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-39-578_-39-577ins others(24): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446319 | |||||
| chr11:76446319
|
G | GTGTATAT others(43): Show |
2 | a0001c0001t0001g0353a0001c0001t0002g0283 | 2 | HG00140.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-39-578_-39-577ins others(50): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446319 | |||||
| chr11:76446321
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39-578_-39-577ins others(28): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446321 | |||||
| chr11:76446323
|
G | A | 4 | a0001c0001t0002g0284a0001c0001t0002g0319a0001c0001t0014g0287others(1): Show | 4 | HG03225.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-577G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446323 | ||||||
| chr11:76446333
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-39-567A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446333 | ||||||
| chr11:76446335
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-39-565G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446335 | ||||||
| chr11:76446345
|
A | G | 3 | a0001c0001t0002g0284a0001c0001t0003g0285a0001c0001t0003g0286 | 3 | HG02258.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-39-555A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446345 | ||||||
| chr11:76446349
|
G | A | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-39-551G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446349 | ||||||
| chr11:76446349
|
G | GTA | 268 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-39-539_-39-538dup others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446349
|
G | GTATA | 5 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0003g0083others(2): Show | 5 | HG03098.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39-541_-39-538dup others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446349
|
G | GTATATA | 27 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(24): Show | 27 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-39-543_-39-538dup others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446349
|
G | GTATATAT others(1): Show |
6 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-545_-39-538dup others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446349
|
G | GTATATAT others(25): Show |
1 | a0001c0001t0001g0322 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-39-540_-39-539ins others(32): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446349
|
GTA | G | 16 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(13): Show | 16 | HG00323.hp1 HG02015.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.-39-539_-39-538del others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 76446349 | |||||
| chr11:76446430
|
C | T | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-39-470C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446430 | ||||||
| chr11:76446445
|
A | C | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-39-455A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446445 | ||||||
| chr11:76446642
|
T | C | 331 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-39-258T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 1/21 | chr11 | 76446642 | ||||||
| chr11:76447391
|
G | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.70+383G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76447391 | ||||||
| chr11:76447592
|
T | C | 331 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.70+584T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76447592 | ||||||
| chr11:76447693
|
G | C | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+685G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76447693 | ||||||
| chr11:76447742
|
A | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+734A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76447742 | ||||||
| chr11:76448040
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.70+1032T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448040 | ||||||
| chr11:76448111
|
T | A | 1 | a0001c0001t0005g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.70+1103T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448111 | ||||||
| chr11:76448144
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.70+1136C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448144 | ||||||
| chr11:76448320
|
G | C | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70+1312G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448320 | ||||||
| chr11:76448468
|
A | G | 1 | a0001c0001t0015g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.70+1460A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448468 | ||||||
| chr11:76448593
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.70+1585G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448593 | ||||||
| chr11:76448641
|
G | A | 33 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(30): Show | 33 | HG00609.hp2 HG01106.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.70+1633G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76448641 | ||||||
| chr11:76449110
|
G | A | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+2102G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449110 | ||||||
| chr11:76449138
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.70+2130A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449138 | ||||||
| chr11:76449154
|
G | A | 331 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.70+2146G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449154 | ||||||
| chr11:76449214
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70+2206G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449214 | ||||||
| chr11:76449260
|
G | A | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.70+2252G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449260 | ||||||
| chr11:76449293
|
A | G | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.70+2285A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449293 | ||||||
| chr11:76449494
|
A | G | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.71-2364A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449494 | ||||||
| chr11:76449501
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.71-2357C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76449501 | ||||||
| chr11:76449941
|
CAT | C | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(2): Show | 5 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1914_71-1913del others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76449941 | |||||
| chr11:76450057
|
CT | C | 319 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.71-1785delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76450057 | |||||
| chr11:76450160
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.71-1698C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450160 | ||||||
| chr11:76450177
|
C | T | 32 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(29): Show | 32 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.71-1681C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450177 | ||||||
| chr11:76450343
|
AAACT | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.71-1509_71-1506del others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76450343 | |||||
| chr11:76450345
|
A | G | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.71-1513A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450345 | ||||||
| chr11:76450678
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71-1180G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450678 | ||||||
| chr11:76450783
|
A | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.71-1075A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450783 | ||||||
| chr11:76450794
|
A | AT | 123 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.71-1047dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76450794 | |||||
| chr11:76450794
|
A | ATT | 16 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0255others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-1048_71-1047dup others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76450794 | |||||
| chr11:76450794
|
A | ATTT | 189 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.71-1049_71-1047dup others(3): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 76450794 | |||||
| chr11:76450814
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.71-1044G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450814 | ||||||
| chr11:76450977
|
T | G | 5 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01192.hp2 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-881T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76450977 | ||||||
| chr11:76451060
|
G | A | 2 | a0001c0001t0005g0110a0001c0001t0005g0111 | 2 | NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.71-798G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451060 | ||||||
| chr11:76451249
|
C | T | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71-609C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451249 | ||||||
| chr11:76451409
|
C | G | 1 | a0001c0001t0002g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.71-449C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451409 | ||||||
| chr11:76451432
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.71-426G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451432 | ||||||
| chr11:76451599
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71-259A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451599 | ||||||
| chr11:76451747
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-111A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451747 | ||||||
| chr11:76451798
|
C | T | 2 | a0001c0003t0001g0247a0001c0003t0001g0248 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.71-60C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451798 | ||||||
| chr11:76451851
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | HG03239.hp1 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.71-7C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 2/21 | chr11 | 76451851 | ||||||
| chr11:76451964
|
T | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.170+7T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76451964 | ||||||
| chr11:76452107
|
T | C | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.170+150T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452107 | ||||||
| chr11:76452294
|
T | C | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170+337T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452294 | ||||||
| chr11:76452372
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.170+415T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452372 | ||||||
| chr11:76452458
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.170+501A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452458 | ||||||
| chr11:76452465
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02717.hp2 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.170+508C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452465 | ||||||
| chr11:76452682
|
T | C | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.171-632T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452682 | ||||||
| chr11:76452734
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.171-580G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452734 | ||||||
| chr11:76452968
|
A | G | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.171-346A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76452968 | ||||||
| chr11:76453105
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.171-209A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76453105 | ||||||
| chr11:76453141
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.171-173T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 3/21 | chr11 | 76453141 | ||||||
| chr11:76453585
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.245+197G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76453585 | ||||||
| chr11:76453615
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.245+227A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76453615 | ||||||
| chr11:76453859
|
A | G | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.245+471A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76453859 | ||||||
| chr11:76453911
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.245+523C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76453911 | ||||||
| chr11:76453915
|
T | G | 120 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.245+527T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76453915 | ||||||
| chr11:76454086
|
G | C | 1 | a0001c0001t0003g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.246-663G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454086 | ||||||
| chr11:76454171
|
A | G | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.246-578A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454171 | ||||||
| chr11:76454243
|
C | T | 120 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.246-506C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454243 | ||||||
| chr11:76454269
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.246-480C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454269 | ||||||
| chr11:76454433
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.246-316G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454433 | ||||||
| chr11:76454509
|
G | A | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.246-240G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454509 | ||||||
| chr11:76454711
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.246-38A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 4/21 | chr11 | 76454711 | ||||||
| chr11:76454947
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.287+157C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76454947 | ||||||
| chr11:76455045
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+255C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76455045 | ||||||
| chr11:76455635
|
A | G | 17 | a0001c0002t0001g0024a0001c0002t0001g0065a0001c0002t0001g0066others(14): Show | 17 | HG00323.hp1 HG02015.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.287+845A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76455635 | ||||||
| chr11:76455841
|
A | G | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.287+1051A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76455841 | ||||||
| chr11:76455984
|
A | G | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287+1194A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76455984 | ||||||
| chr11:76456060
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.287+1270G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456060 | ||||||
| chr11:76456418
|
C | T | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.287+1628C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456418 | ||||||
| chr11:76456431
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.287+1641G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456431 | ||||||
| chr11:76456557
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.288-1626G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456557 | ||||||
| chr11:76456687
|
C | T | 1 | a0001c0002t0010g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.288-1496C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456687 | ||||||
| chr11:76456899
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-1284T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76456899 | ||||||
| chr11:76457175
|
C | T | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.288-1008C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457175 | ||||||
| chr11:76457176
|
C | A | 1 | a0001c0001t0002g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.288-1007C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457176 | ||||||
| chr11:76457540
|
T | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.288-643T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457540 | ||||||
| chr11:76457665
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-518G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457665 | ||||||
| chr11:76457692
|
C | G | 1 | a0001c0001t0020g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.288-491C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457692 | ||||||
| chr11:76457717
|
G | T | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.288-466G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76457717 | ||||||
| chr11:76458053
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.288-130A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76458053 | ||||||
| chr11:76458110
|
T | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.288-73T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 5/21 | chr11 | 76458110 | ||||||
| chr11:76458600
|
A | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.463+242A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76458600 | ||||||
| chr11:76458864
|
C | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.463+506C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76458864 | ||||||
| chr11:76458906
|
A | T | 1 | a0001c0002t0001g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.463+548A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76458906 | ||||||
| chr11:76459039
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.463+681G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459039 | ||||||
| chr11:76459062
|
G | T | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.463+704G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459062 | ||||||
| chr11:76459146
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.464-787G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459146 | ||||||
| chr11:76459146
|
G | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.464-787G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459146 | ||||||
| chr11:76459363
|
A | G | 4 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 4 | NA18988.hp2 NA18999.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-570A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459363 | ||||||
| chr11:76459392
|
C | T | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464-541C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459392 | ||||||
| chr11:76459608
|
G | C | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.464-325G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459608 | ||||||
| chr11:76459643
|
C | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-290C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 6/21 | chr11 | 76459643 | ||||||
| chr11:76460218
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.616+133A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460218 | ||||||
| chr11:76460237
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.616+152A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460237 | ||||||
| chr11:76460374
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.616+289A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460374 | ||||||
| chr11:76460406
|
G | A | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.616+321G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460406 | ||||||
| chr11:76460851
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.616+766G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460851 | ||||||
| chr11:76460891
|
G | C | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.616+806G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460891 | ||||||
| chr11:76460914
|
C | T | 1 | a0001c0001t0013g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.616+829C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460914 | ||||||
| chr11:76460920
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.616+835G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460920 | ||||||
| chr11:76460938
|
C | T | 1 | a0001c0001t0015g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.616+853C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76460938 | ||||||
| chr11:76461330
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.616+1245T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461330 | ||||||
| chr11:76461339
|
T | C | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.616+1254T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461339 | ||||||
| chr11:76461438
|
G | T | 6 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0025others(3): Show | 6 | HG01261.hp1 HG01433.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.616+1353G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461438 | ||||||
| chr11:76461564
|
T | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.616+1479T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461564 | ||||||
| chr11:76461729
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.616+1644C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461729 | ||||||
| chr11:76461782
|
A | C | 3 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109 | 3 | NA18949.hp1 NA18984.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.616+1697A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461782 | ||||||
| chr11:76461996
|
G | A | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.617-1825G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76461996 | ||||||
| chr11:76462003
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.617-1818G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462003 | ||||||
| chr11:76462058
|
G | A | 1 | a0001c0001t0009g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.617-1763G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462058 | ||||||
| chr11:76462098
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-1723G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462098 | ||||||
| chr11:76462155
|
C | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.617-1666C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462155 | ||||||
| chr11:76462191
|
A | G | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18997.hp1 NA19085.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.617-1630A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462191 | ||||||
| chr11:76462193
|
C | T | 120 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.617-1628C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462193 | ||||||
| chr11:76462310
|
A | T | 1 | a0001c0001t0002g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.617-1511A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462310 | ||||||
| chr11:76462353
|
A | G | 2 | a0001c0003t0001g0252a0001c0003t0001g0253 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.617-1468A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462353 | ||||||
| chr11:76462402
|
A | G | 1 | a0001c0001t0002g0178 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.617-1419A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462402 | ||||||
| chr11:76462403
|
A | C | 1 | a0001c0001t0020g0240 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.617-1418A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462403 | ||||||
| chr11:76462426
|
A | G | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.617-1395A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462426 | ||||||
| chr11:76462446
|
A | G | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.617-1375A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462446 | ||||||
| chr11:76462606
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.617-1215T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462606 | ||||||
| chr11:76462904
|
A | G | 4 | a0001c0001t0002g0276a0001c0001t0002g0278a0001c0001t0009g0002others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-917A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462904 | ||||||
| chr11:76462905
|
G | C | 1 | a0001c0001t0002g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.617-916G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462905 | ||||||
| chr11:76462962
|
G | A | 1 | a0001c0001t0006g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.617-859G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76462962 | ||||||
| chr11:76463051
|
C | T | 70 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.617-770C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463051 | ||||||
| chr11:76463146
|
G | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-675G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463146 | ||||||
| chr11:76463279
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.617-542C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463279 | ||||||
| chr11:76463323
|
AAAAG | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.617-493_617-490del others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 76463323 | |||||
| chr11:76463344
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.617-477C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463344 | ||||||
| chr11:76463351
|
C | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.617-470C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463351 | ||||||
| chr11:76463372
|
C | A | 1 | a0001c0002t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.617-449C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463372 | ||||||
| chr11:76463397
|
G | A | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.617-424G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463397 | ||||||
| chr11:76463515
|
C | T | 1 | a0001c0001t0002g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.617-306C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463515 | ||||||
| chr11:76463547
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-274C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463547 | ||||||
| chr11:76463548
|
G | T | 1 | a0001c0002t0001g0027 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.617-273G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463548 | ||||||
| chr11:76463563
|
C | G | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.617-258C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463563 | ||||||
| chr11:76463580
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.617-241G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | chr11 | 76463580 | ||||||
| chr11:76463629
|
C | CA | 78 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(75): Show | 79 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.617-173dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 76463629 | |||||
| chr11:76463629
|
CA | C | 23 | a0001c0001t0002g0234a0001c0001t0002g0273a0001c0001t0003g0235others(20): Show | 23 | HG00323.hp2 HG00597.hp2 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.617-173delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 76463629 | |||||
| chr11:76463629
|
CAA | C | 70 | a0001c0001t0002g0115a0001c0002t0001g0005a0001c0002t0001g0006others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.617-174_617-173del others(2): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 76463629 | |||||
| chr11:76464223
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.876+143A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76464223 | ||||||
| chr11:76464462
|
C | T | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.876+382C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76464462 | ||||||
| chr11:76464751
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.876+671C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76464751 | ||||||
| chr11:76465007
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+927T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465007 | ||||||
| chr11:76465067
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | NA18948.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.876+987G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465067 | ||||||
| chr11:76465216
|
A | G | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.876+1136A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465216 | ||||||
| chr11:76465356
|
C | G | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+1276C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465356 | ||||||
| chr11:76465381
|
G | A | 354 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.876+1301G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465381 | ||||||
| chr11:76465392
|
A | G | 1 | a0001c0001t0003g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.876+1312A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465392 | ||||||
| chr11:76465966
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.876+1886A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76465966 | ||||||
| chr11:76466052
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.876+1972C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466052 | ||||||
| chr11:76466065
|
A | G | 1 | a0001c0001t0002g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.876+1985A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466065 | ||||||
| chr11:76466067
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.876+1987A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466067 | ||||||
| chr11:76466115
|
C | G | 1 | a0001c0001t0001g0312 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.876+2035C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466115 | ||||||
| chr11:76466144
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.876+2064T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466144 | ||||||
| chr11:76466371
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.876+2291T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466371 | ||||||
| chr11:76466375
|
C | T | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.876+2295C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466375 | ||||||
| chr11:76466486
|
T | TA | 15 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.876+2415dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 76466486 | |||||
| chr11:76466677
|
A | G | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.876+2597A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466677 | ||||||
| chr11:76466861
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.876+2781T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466861 | ||||||
| chr11:76466947
|
T | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0020 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.876+2867T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76466947 | ||||||
| chr11:76467066
|
A | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.876+2986A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467066 | ||||||
| chr11:76467074
|
A | C | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.876+2994A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467074 | ||||||
| chr11:76467191
|
T | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.876+3111T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467191 | ||||||
| chr11:76467406
|
A | G | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.876+3326A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467406 | ||||||
| chr11:76467628
|
G | T | 54 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(51): Show | 54 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.876+3548G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467628 | ||||||
| chr11:76467767
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+3687G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467767 | ||||||
| chr11:76467848
|
C | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.876+3768C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467848 | ||||||
| chr11:76467979
|
CA | C | 100 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(97): Show | 100 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.876+3911delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 76467979 | |||||
| chr11:76467990
|
A | C | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.876+3910A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467990 | ||||||
| chr11:76467991
|
A | C | 206 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.876+3911A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467991 | ||||||
| chr11:76467992
|
C | A | 206 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.876+3912C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467992 | ||||||
| chr11:76467993
|
A | C | 1 | a0001c0002t0001g0032 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.876+3913A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467993 | ||||||
| chr11:76467994
|
A | C | 1 | a0001c0001t0007g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.876+3914A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467994 | ||||||
| chr11:76467995
|
A | C | 3 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | NA18979.hp1 NA19001.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.876+3915A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467995 | ||||||
| chr11:76467996
|
A | C | 6 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+3916A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76467996 | ||||||
| chr11:76468013
|
G | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.876+3933G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468013 | ||||||
| chr11:76468072
|
C | T | 120 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.876+3992C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468072 | ||||||
| chr11:76468304
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.876+4224T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468304 | ||||||
| chr11:76468436
|
G | T | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.877-4128G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468436 | ||||||
| chr11:76468503
|
T | C | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.877-4061T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468503 | ||||||
| chr11:76468794
|
G | A | 4 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.877-3770G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76468794 | ||||||
| chr11:76469038
|
T | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-3526T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469038 | ||||||
| chr11:76469047
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.877-3517A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469047 | ||||||
| chr11:76469245
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.877-3319A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469245 | ||||||
| chr11:76469392
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.877-3172A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469392 | ||||||
| chr11:76469446
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.877-3118A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469446 | ||||||
| chr11:76469624
|
G | A | 357 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.877-2940G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469624 | ||||||
| chr11:76469626
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.877-2938G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76469626 | ||||||
| chr11:76470207
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.877-2357G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470207 | ||||||
| chr11:76470289
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.877-2275G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470289 | ||||||
| chr11:76470430
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-2134T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470430 | ||||||
| chr11:76470587
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0260a0001c0001t0002g0261others(5): Show | 9 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.877-1977G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470587 | ||||||
| chr11:76470597
|
G | A | 1 | a0001c0001t0011g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877-1967G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470597 | ||||||
| chr11:76470783
|
T | C | 1 | a0001c0001t0002g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.877-1781T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470783 | ||||||
| chr11:76470929
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.877-1635T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76470929 | ||||||
| chr11:76471074
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-1490T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76471074 | ||||||
| chr11:76471144
|
A | T | 1 | a0001c0001t0011g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877-1420A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76471144 | ||||||
| chr11:76471278
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.877-1286G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76471278 | ||||||
| chr11:76471349
|
C | T | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.877-1215C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76471349 | ||||||
| chr11:76471947
|
C | A | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | NA18940.hp1 NA18968.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.877-617C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76471947 | ||||||
| chr11:76472058
|
CTTT | C | 118 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(115): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.877-502_877-500del others(3): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 76472058 | |||||
| chr11:76472062
|
T | A | 119 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.877-502T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472062 | ||||||
| chr11:76472063
|
T | A | 119 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.877-501T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472063 | ||||||
| chr11:76472064
|
T | A | 119 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.877-500T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472064 | ||||||
| chr11:76472176
|
T | A | 1 | a0001c0001t0003g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.877-388T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472176 | ||||||
| chr11:76472314
|
A | G | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877-250A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472314 | ||||||
| chr11:76472336
|
G | A | 1 | a0001c0001t0008g0188 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.877-228G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 8/21 | chr11 | 76472336 | ||||||
| chr11:76472880
|
A | G | 209 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1153+40A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76472880 | ||||||
| chr11:76472942
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1153+102C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76472942 | ||||||
| chr11:76472967
|
G | A | 326 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1153+127G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76472967 | ||||||
| chr11:76473008
|
A | G | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1153+168A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473008 | ||||||
| chr11:76473253
|
T | A | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1153+413T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473253 | ||||||
| chr11:76473337
|
C | T | 1 | a0001c0002t0010g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1153+497C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473337 | ||||||
| chr11:76473511
|
G | T | 9 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153+671G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473511 | ||||||
| chr11:76473555
|
C | T | 78 | a0001c0001t0002g0008a0001c0001t0002g0089a0001c0001t0002g0092others(75): Show | 78 | HG00408.hp2 HG01099.hp2 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.1153+715C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473555 | ||||||
| chr11:76473569
|
G | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+729G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473569 | ||||||
| chr11:76473590
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1153+750C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473590 | ||||||
| chr11:76473619
|
A | G | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+779A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473619 | ||||||
| chr11:76473671
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0080 | 2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1153+831C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473671 | ||||||
| chr11:76473703
|
G | C | 1 | a0001c0002t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1153+863G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473703 | ||||||
| chr11:76473800
|
G | A | 7 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0001t0002g0141others(4): Show | 7 | NA18942.hp2 NA18947.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+960G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473800 | ||||||
| chr11:76473900
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1060C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76473900 | ||||||
| chr11:76474074
|
G | T | 1 | a0001c0001t0002g0270 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1153+1234G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76474074 | ||||||
| chr11:76474108
|
C | A | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1153+1268C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76474108 | ||||||
| chr11:76474115
|
C | CA | 249 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1153+1291dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76474115 | |||||
| chr11:76474115
|
C | CAA | 7 | a0001c0001t0001g0322a0001c0001t0002g0119a0001c0001t0002g0141others(4): Show | 7 | HG00597.hp2 HG01071.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+1290_1153+129 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76474115 | |||||
| chr11:76474115
|
CA | C | 14 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0069others(11): Show | 14 | HG00323.hp1 HG02040.hp1 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.1153+1291delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76474115 | |||||
| chr11:76474330
|
A | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1153+1490A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76474330 | ||||||
| chr11:76474944
|
A | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+2104A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76474944 | ||||||
| chr11:76475059
|
C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1153+2219C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475059 | ||||||
| chr11:76475060
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1153+2220G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475060 | ||||||
| chr11:76475106
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+2266G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475106 | ||||||
| chr11:76475531
|
A | G | 2 | a0001c0002t0001g0078a0001c0002t0021g0079 | 2 | NA18965.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1153+2691A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475531 | ||||||
| chr11:76475624
|
T | G | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1153+2784T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475624 | ||||||
| chr11:76475752
|
C | T | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1153+2912C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475752 | ||||||
| chr11:76475793
|
G | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | NA18992.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1153+2953G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475793 | ||||||
| chr11:76475915
|
A | G | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1153+3075A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76475915 | ||||||
| chr11:76476106
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+3266A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76476106 | ||||||
| chr11:76476695
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+3855A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76476695 | ||||||
| chr11:76476749
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+3909C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76476749 | ||||||
| chr11:76476809
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1153+3969G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76476809 | ||||||
| chr11:76476874
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+4034T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76476874 | ||||||
| chr11:76477050
|
A | C | 1 | a0001c0001t0002g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1153+4210A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477050 | ||||||
| chr11:76477083
|
T | G | 1 | a0001c0002t0022g0022 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1153+4243T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477083 | ||||||
| chr11:76477270
|
G | GT | 32 | a0001c0001t0002g0113a0001c0001t0003g0229a0001c0002t0001g0005others(29): Show | 32 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1153+4441dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76477270 | |||||
| chr11:76477330
|
A | G | 1 | a0001c0001t0004g0100 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1153+4490A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477330 | ||||||
| chr11:76477503
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1153+4663A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477503 | ||||||
| chr11:76477507
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+4667G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477507 | ||||||
| chr11:76477592
|
T | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+4752T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477592 | ||||||
| chr11:76477738
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1153+4898G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477738 | ||||||
| chr11:76477769
|
T | C | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1153+4929T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477769 | ||||||
| chr11:76477786
|
A | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+4946A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477786 | ||||||
| chr11:76477817
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1153+4977G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76477817 | ||||||
| chr11:76478005
|
C | T | 2 | a0001c0001t0013g0118a0001c0001t0013g0320 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1153+5165C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478005 | ||||||
| chr11:76478041
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0002g0283 | 2 | HG00140.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1153+5201C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478041 | ||||||
| chr11:76478160
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1153+5320T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478160 | ||||||
| chr11:76478340
|
A | AT | 22 | a0001c0001t0001g0311a0001c0001t0001g0350a0001c0001t0002g0113others(19): Show | 22 | HG00733.hp1 HG01192.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1153+5521dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76478340 | |||||
| chr11:76478340
|
AT | A | 95 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0316others(92): Show | 95 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1153+5521delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76478340 | |||||
| chr11:76478398
|
C | T | 1 | a0001c0001t0005g0220 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1153+5558C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478398 | ||||||
| chr11:76478671
|
A | C | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1153+5831A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478671 | ||||||
| chr11:76478841
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153+6001C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478841 | ||||||
| chr11:76478993
|
T | C | 1 | a0001c0001t0003g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1153+6153T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76478993 | ||||||
| chr11:76479010
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1153+6170C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479010 | ||||||
| chr11:76479168
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+6328C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479168 | ||||||
| chr11:76479289
|
T | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1153+6449T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479289 | ||||||
| chr11:76479306
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0352 | 3 | HG01884.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1153+6466C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479306 | ||||||
| chr11:76479339
|
A | G | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1153+6499A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479339 | ||||||
| chr11:76479475
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+6635C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479475 | ||||||
| chr11:76479479
|
A | G | 1 | a0001c0002t0001g0047 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1153+6639A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479479 | ||||||
| chr11:76479728
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1153+6888C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479728 | ||||||
| chr11:76479808
|
A | G | 1 | a0001c0001t0002g0117 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1153+6968A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479808 | ||||||
| chr11:76479823
|
A | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+6983A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479823 | ||||||
| chr11:76479842
|
G | A | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(2): Show | 5 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+7002G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76479842 | ||||||
| chr11:76480445
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1153+7605G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480445 | ||||||
| chr11:76480470
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1153+7630A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480470 | ||||||
| chr11:76480517
|
G | A | 4 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0002g0135others(1): Show | 4 | HG01346.hp2 HG02559.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+7677G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480517 | ||||||
| chr11:76480593
|
A | G | 209 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1153+7753A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480593 | ||||||
| chr11:76480711
|
G | C | 1 | a0001c0001t0001g0352 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1153+7871G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480711 | ||||||
| chr11:76480928
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+8088A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480928 | ||||||
| chr11:76480935
|
T | G | 4 | a0001c0001t0002g0255a0001c0001t0002g0260a0001c0001t0002g0261others(1): Show | 4 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+8095T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480935 | ||||||
| chr11:76480941
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+8101G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480941 | ||||||
| chr11:76480992
|
G | A | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1153+8152G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76480992 | ||||||
| chr11:76481007
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1153+8167G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481007 | ||||||
| chr11:76481104
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1153+8264C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481104 | ||||||
| chr11:76481201
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1153+8361G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481201 | ||||||
| chr11:76481264
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+8424C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481264 | ||||||
| chr11:76481285
|
C | T | 120 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1153+8445C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481285 | ||||||
| chr11:76481288
|
C | T | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1153+8448C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481288 | ||||||
| chr11:76481340
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0313 | 2 | HG00621.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1153+8500G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481340 | ||||||
| chr11:76481478
|
C | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+8638C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481478 | ||||||
| chr11:76481637
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1153+8797C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481637 | ||||||
| chr11:76481742
|
C | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+8902C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76481742 | ||||||
| chr11:76482048
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1153+9208A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482048 | ||||||
| chr11:76482153
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1153+9313A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482153 | ||||||
| chr11:76482301
|
C | T | 2 | a0001c0001t0002g0283a0001c0002t0001g0024 | 2 | HG00140.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1153+9461C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482301 | ||||||
| chr11:76482454
|
G | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG00544.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1153+9614G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482454 | ||||||
| chr11:76482501
|
G | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1153+9661G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482501 | ||||||
| chr11:76482569
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1153+9729G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482569 | ||||||
| chr11:76482770
|
G | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+9930G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482770 | ||||||
| chr11:76482871
|
G | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153+10031G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482871 | ||||||
| chr11:76482926
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1153+10086G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482926 | ||||||
| chr11:76482949
|
G | A | 1 | a0001c0003t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153+10109G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482949 | ||||||
| chr11:76482951
|
C | G | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1153+10111C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76482951 | ||||||
| chr11:76483416
|
A | G | 1 | a0001c0002t0010g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1153+10576A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483416 | ||||||
| chr11:76483481
|
C | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+10641C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483481 | ||||||
| chr11:76483486
|
G | A | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1153+10646G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483486 | ||||||
| chr11:76483645
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+10805G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483645 | ||||||
| chr11:76483678
|
C | A | 1 | a0001c0003t0001g0247 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1153+10838C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483678 | ||||||
| chr11:76483850
|
A | G | 25 | a0001c0001t0002g0008a0001c0001t0002g0093a0001c0001t0002g0105others(22): Show | 25 | HG01175.hp1 HG01192.hp2 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.1153+11010A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483850 | ||||||
| chr11:76483949
|
C | T | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1153+11109C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76483949 | ||||||
| chr11:76484023
|
A | G | 2 | a0001c0003t0001g0247a0001c0003t0001g0248 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1153+11183A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76484023 | ||||||
| chr11:76484477
|
G | A | 324 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1153+11637G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76484477 | ||||||
| chr11:76484628
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0003g0238 | 2 | NA18956.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1154-11587C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76484628 | ||||||
| chr11:76484733
|
G | T | 1 | a0001c0001t0001g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1154-11482G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76484733 | ||||||
| chr11:76484928
|
C | CA | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0170others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1154-11272dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76484928 | |||||
| chr11:76484928
|
CA | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-11272delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76484928 | |||||
| chr11:76484937
|
A | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-11278A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76484937 | ||||||
| chr11:76485080
|
C | T | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1154-11135C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485080 | ||||||
| chr11:76485282
|
A | G | 6 | a0001c0001t0001g0322a0001c0001t0001g0336a0001c0001t0001g0337others(3): Show | 6 | HG01071.hp2 HG02165.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-10933A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485282 | ||||||
| chr11:76485391
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1154-10824C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485391 | ||||||
| chr11:76485498
|
C | T | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1154-10717C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485498 | ||||||
| chr11:76485522
|
A | G | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1154-10693A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485522 | ||||||
| chr11:76485541
|
G | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1154-10674G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485541 | ||||||
| chr11:76485701
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1154-10514A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485701 | ||||||
| chr11:76485800
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1154-10415G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485800 | ||||||
| chr11:76485888
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1154-10327A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485888 | ||||||
| chr11:76485948
|
A | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1154-10267A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76485948 | ||||||
| chr11:76486158
|
A | G | 6 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0025others(3): Show | 6 | HG01261.hp1 HG01433.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-10057A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486158 | ||||||
| chr11:76486169
|
A | C | 326 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1154-10046A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486169 | ||||||
| chr11:76486272
|
G | T | 1 | a0001c0001t0003g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1154-9943G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486272 | ||||||
| chr11:76486574
|
A | G | 12 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG00323.hp2 HG00597.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1154-9641A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486574 | ||||||
| chr11:76486704
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1154-9511G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486704 | ||||||
| chr11:76486724
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154-9491G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486724 | ||||||
| chr11:76486853
|
T | C | 1 | a0001c0003t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1154-9362T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486853 | ||||||
| chr11:76486931
|
C | G | 1 | a0001c0001t0002g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1154-9284C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76486931 | ||||||
| chr11:76487001
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-9214G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487001 | ||||||
| chr11:76487048
|
C | A | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1154-9167C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487048 | ||||||
| chr11:76487273
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1154-8942G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487273 | ||||||
| chr11:76487517
|
G | A | 4 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0002g0135others(1): Show | 4 | HG01346.hp2 HG02559.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-8698G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487517 | ||||||
| chr11:76487576
|
G | A | 208 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1154-8639G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487576 | ||||||
| chr11:76487642
|
C | T | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1154-8573C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487642 | ||||||
| chr11:76487722
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1154-8493G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487722 | ||||||
| chr11:76487797
|
C | T | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-8418C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487797 | ||||||
| chr11:76487821
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1154-8394A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487821 | ||||||
| chr11:76487834
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1154-8381T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487834 | ||||||
| chr11:76487899
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-8316C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487899 | ||||||
| chr11:76487948
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327 | 3 | HG02922.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1154-8267G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76487948 | ||||||
| chr11:76488018
|
A | G | 1 | a0001c0001t0027g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1154-8197A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488018 | ||||||
| chr11:76488024
|
C | G | 1 | a0001c0001t0001g0308 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1154-8191C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488024 | ||||||
| chr11:76488153
|
T | G | 1 | a0001c0001t0001g0336 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1154-8062T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488153 | ||||||
| chr11:76488170
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1154-8045G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488170 | ||||||
| chr11:76488189
|
A | G | 313 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1154-8026A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488189 | ||||||
| chr11:76488332
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1154-7883G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488332 | ||||||
| chr11:76488350
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1154-7865T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488350 | ||||||
| chr11:76488440
|
C | A | 194 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1154-7775C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488440 | ||||||
| chr11:76488481
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1154-7734T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488481 | ||||||
| chr11:76488524
|
AT | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(249): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1154-7681delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76488524 | |||||
| chr11:76488533
|
T | TG | 4 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0022g0022others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-7682_1154-768 others(5): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488533 | ||||||
| chr11:76488534
|
T | G | 70 | a0001c0001t0002g0093a0001c0001t0002g0254a0001c0001t0018g0084others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1154-7681T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488534 | ||||||
| chr11:76488535
|
G | T | 74 | a0001c0001t0002g0093a0001c0001t0002g0254a0001c0001t0018g0084others(71): Show | 74 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1154-7680G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488535 | ||||||
| chr11:76488660
|
T | C | 4 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0022g0022others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-7555T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488660 | ||||||
| chr11:76488749
|
A | C | 1 | a0001c0001t0012g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1154-7466A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76488749 | ||||||
| chr11:76489040
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154-7175T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489040 | ||||||
| chr11:76489095
|
C | G | 1 | a0001c0001t0003g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1154-7120C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489095 | ||||||
| chr11:76489272
|
C | T | 5 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0101others(2): Show | 5 | NA18970.hp2 NA18997.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-6943C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489272 | ||||||
| chr11:76489309
|
T | C | 1 | a0001c0001t0013g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1154-6906T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489309 | ||||||
| chr11:76489315
|
CT | C | 103 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1154-6883delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76489315 | |||||
| chr11:76489462
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1154-6753T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489462 | ||||||
| chr11:76489608
|
C | CT | 219 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(216): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1154-6593dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76489608 | |||||
| chr11:76489680
|
C | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-6535C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489680 | ||||||
| chr11:76489838
|
C | T | 72 | a0001c0001t0002g0254a0001c0002t0001g0005a0001c0002t0001g0006others(69): Show | 72 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1154-6377C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489838 | ||||||
| chr11:76489901
|
G | A | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1154-6314G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489901 | ||||||
| chr11:76489915
|
A | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-6300A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76489915 | ||||||
| chr11:76490070
|
C | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1154-6145C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490070 | ||||||
| chr11:76490076
|
G | A | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1154-6139G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490076 | ||||||
| chr11:76490135
|
T | A | 6 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-6080T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490135 | ||||||
| chr11:76490183
|
A | AT | 10 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(7): Show | 10 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-6022dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76490183 | |||||
| chr11:76490221
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1154-5994G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490221 | ||||||
| chr11:76490268
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1154-5947A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490268 | ||||||
| chr11:76490420
|
T | C | 1 | a0001c0002t0001g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1154-5795T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490420 | ||||||
| chr11:76490577
|
C | T | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-5638C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490577 | ||||||
| chr11:76490727
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-5488G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490727 | ||||||
| chr11:76490853
|
G | GGT | 6 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0278others(3): Show | 6 | HG01256.hp1 HG02818.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-5361_1154-536 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76490853 | |||||
| chr11:76490855
|
G | GGT | 6 | a0001c0001t0011g0082a0001c0001t0014g0287a0001c0001t0014g0288others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-5335_1154-533 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76490855 | |||||
| chr11:76490855
|
G | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1154-5360G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490855 | ||||||
| chr11:76490855
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0001g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1154-5343_1154-533 others(14): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76490855 | |||||
| chr11:76490908
|
A | G | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1154-5307A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76490908 | ||||||
| chr11:76491177
|
C | CT | 73 | a0001c0001t0001g0296a0001c0001t0001g0307a0001c0001t0001g0323others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1154-5020dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76491177 | |||||
| chr11:76491177
|
CT | C | 88 | a0001c0001t0001g0291a0001c0001t0001g0297a0001c0001t0001g0298others(85): Show | 88 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1154-5020delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76491177 | |||||
| chr11:76491177
|
CTT | C | 6 | a0001c0002t0001g0038a0001c0002t0001g0077a0001c0003t0001g0247others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-5021_1154-502 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76491177 | |||||
| chr11:76491384
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1154-4831G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491384 | ||||||
| chr11:76491453
|
T | G | 1 | a0001c0001t0005g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1154-4762T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491453 | ||||||
| chr11:76491480
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-4735C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491480 | ||||||
| chr11:76491481
|
C | T | 4 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0237others(1): Show | 4 | NA18952.hp1 NA18956.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-4734C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491481 | ||||||
| chr11:76491560
|
G | T | 1 | a0001c0001t0002g0137 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1154-4655G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491560 | ||||||
| chr11:76491601
|
G | C | 1 | a0001c0001t0002g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1154-4614G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491601 | ||||||
| chr11:76491664
|
C | T | 1 | a0001c0001t0006g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1154-4551C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491664 | ||||||
| chr11:76491739
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1154-4476C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491739 | ||||||
| chr11:76491754
|
G | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0292a0001c0001t0001g0293others(8): Show | 12 | HG00544.hp2 NA18747.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154-4461G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491754 | ||||||
| chr11:76491754
|
G | T | 15 | a0001c0001t0001g0291a0001c0001t0001g0294a0001c0001t0001g0295others(12): Show | 15 | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1154-4461G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491754 | ||||||
| chr11:76491830
|
A | G | 2 | a0001c0002t0001g0006a0001c0002t0001g0007 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1154-4385A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491830 | ||||||
| chr11:76491868
|
G | T | 1 | a0001c0001t0003g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1154-4347G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76491868 | ||||||
| chr11:76492248
|
T | C | 2 | a0001c0001t0002g0262a0001c0001t0002g0270 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1154-3967T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492248 | ||||||
| chr11:76492572
|
A | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1154-3643A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492572 | ||||||
| chr11:76492590
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1154-3625C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492590 | ||||||
| chr11:76492610
|
G | A | 2 | a0001c0003t0001g0247a0001c0003t0001g0248 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1154-3605G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492610 | ||||||
| chr11:76492627
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1154-3588G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492627 | ||||||
| chr11:76492868
|
G | T | 10 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-3347G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76492868 | ||||||
| chr11:76493032
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1154-3183G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493032 | ||||||
| chr11:76493068
|
C | A | 1 | a0001c0001t0006g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1154-3147C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493068 | ||||||
| chr11:76493297
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1154-2918C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493297 | ||||||
| chr11:76493337
|
G | A | 118 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(115): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1154-2878G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493337 | ||||||
| chr11:76493472
|
T | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1154-2743T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493472 | ||||||
| chr11:76493476
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1154-2739G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493476 | ||||||
| chr11:76493821
|
C | T | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-2394C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493821 | ||||||
| chr11:76493974
|
T | A | 194 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1154-2241T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76493974 | ||||||
| chr11:76494036
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1154-2179G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494036 | ||||||
| chr11:76494615
|
T | TTGCC | 5 | a0001c0002t0001g0020a0001c0002t0001g0024a0001c0002t0001g0071others(2): Show | 5 | HG02886.hp1 HG06807.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-1586_1154-158 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494615 | |||||
| chr11:76494633
|
T | G | 66 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1154-1582T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494633 | ||||||
| chr11:76494636
|
TC | T | 66 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1154-1578delC | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494636 | ||||||
| chr11:76494642
|
T | C | 66 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1154-1573T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494642 | ||||||
| chr11:76494649
|
CCCTT | C | 10 | a0001c0001t0001g0323a0001c0001t0001g0336a0001c0001t0001g0340others(7): Show | 10 | HG02027.hp2 HG02165.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-1481_1154-147 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(1): Show |
C | 14 | a0001c0001t0001g0338a0001c0001t0001g0343a0001c0001t0001g0352others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1154-1485_1154-147 others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(5): Show |
C | 34 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0333others(31): Show | 35 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1154-1489_1154-147 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(9): Show |
C | 48 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0325others(45): Show | 48 | HG01106.hp2 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.1154-1493_1154-147 others(20): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(13): Show |
C | 36 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0001g0335others(33): Show | 36 | HG00597.hp2 HG00609.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.1154-1497_1154-147 others(24): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(17): Show |
C | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0002g0008others(26): Show | 29 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.1154-1501_1154-147 others(28): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(21): Show |
C | 32 | a0001c0001t0002g0004a0001c0001t0002g0104a0001c0001t0002g0160others(29): Show | 32 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1154-1505_1154-147 others(32): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(25): Show |
C | 38 | a0001c0001t0001g0318a0001c0001t0002g0085a0001c0001t0002g0189others(35): Show | 38 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1154-1509_1154-147 others(36): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(29): Show |
C | 9 | a0001c0001t0002g0089a0001c0001t0002g0214a0001c0001t0002g0264others(6): Show | 9 | HG00544.hp1 HG01433.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1154-1513_1154-147 others(40): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494649
|
CCCTTCCT others(33): Show |
C | 4 | a0001c0001t0003g0192a0001c0001t0003g0286a0001c0001t0014g0287others(1): Show | 4 | HG02258.hp1 HG03453.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-1517_1154-147 others(44): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494649 | |||||
| chr11:76494651
|
C | T | 66 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1154-1564C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494651 | ||||||
| chr11:76494654
|
CCTTCCTT | C | 11 | a0001c0002t0001g0015a0001c0002t0001g0027a0001c0002t0001g0035others(8): Show | 11 | HG01358.hp1 HG01496.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.1154-1559_1154-155 others(11): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(4): Show |
C | 8 | a0001c0002t0001g0032a0001c0002t0001g0036a0001c0002t0001g0049others(5): Show | 8 | HG00735.hp1 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154-1559_1154-154 others(15): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(8): Show |
C | 12 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(9): Show | 12 | HG00741.hp1 HG01243.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1154-1559_1154-154 others(19): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(12): Show |
C | 16 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0028others(13): Show | 16 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.1154-1559_1154-154 others(23): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(16): Show |
C | 8 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0021others(5): Show | 8 | HG00438.hp1 HG01070.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154-1559_1154-153 others(27): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(20): Show |
C | 7 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0031others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154-1559_1154-153 others(31): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494654
|
CCTTCCTT others(24): Show |
C | 2 | a0001c0002t0001g0037a0001c0002t0001g0039 | 2 | HG01975.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1154-1559_1154-152 others(35): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494654 | |||||
| chr11:76494675
|
CTTCCTTC others(54): Show |
C | 1 | a0001c0001t0027g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1154-1525_1154-146 others(65): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494675 | |||||
| chr11:76494679
|
CTTCCTTC others(50): Show |
C | 12 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0294others(9): Show | 13 | HG00544.hp2 HG00673.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1154-1521_1154-146 others(61): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494679 | |||||
| chr11:76494683
|
CTTCCTTC others(46): Show |
C | 10 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0297others(7): Show | 10 | HG00621.hp1 HG03017.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154-1517_1154-146 others(57): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494683 | |||||
| chr11:76494687
|
C | A | 1 | a0001c0002t0001g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1154-1528C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494687 | ||||||
| chr11:76494687
|
CTTCCTTC others(42): Show |
C | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0303 | 3 | HG00280.hp1 NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1154-1513_1154-146 others(53): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494687 | |||||
| chr11:76494706
|
CCTTCCTT others(25): Show |
C | 1 | a0001c0002t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1154-1507_1154-147 others(36): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494706 | |||||
| chr11:76494712
|
TTCCTTCC others(12): Show |
T | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1154-1501_1154-148 others(23): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76494712 | |||||
| chr11:76494988
|
A | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1154-1227A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76494988 | ||||||
| chr11:76495015
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-1200C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495015 | ||||||
| chr11:76495031
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-1184C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495031 | ||||||
| chr11:76495285
|
GA | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1154-924delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 76495285 | |||||
| chr11:76495427
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1154-788T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495427 | ||||||
| chr11:76495689
|
A | T | 1 | a0001c0001t0003g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1154-526A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495689 | ||||||
| chr11:76495834
|
G | T | 1 | a0001c0001t0008g0190 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1154-381G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495834 | ||||||
| chr11:76495863
|
C | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1154-352C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76495863 | ||||||
| chr11:76496153
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1154-62C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76496153 | ||||||
| chr11:76496155
|
G | C | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1154-60G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76496155 | ||||||
| chr11:76496194
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1154-21T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 9/21 | chr11 | 76496194 | ||||||
| chr11:76496547
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1408+78G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76496547 | ||||||
| chr11:76496589
|
G | A | 321 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1408+120G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76496589 | ||||||
| chr11:76496665
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1408+196G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76496665 | ||||||
| chr11:76496866
|
A | C | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1408+397A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76496866 | ||||||
| chr11:76496873
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1408+404G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76496873 | ||||||
| chr11:76496993
|
GT | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1408+529delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76496993 | |||||
| chr11:76497345
|
G | A | 77 | a0001c0001t0002g0008a0001c0001t0002g0089a0001c0001t0002g0092others(74): Show | 77 | HG00408.hp2 HG01099.hp2 HG01175.hp1 others(74): Show |
intron_variant | MODIFIER | c.1408+876G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497345 | ||||||
| chr11:76497382
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1408+913G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497382 | ||||||
| chr11:76497407
|
G | A | 71 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(68): Show | 71 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1408+938G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497407 | ||||||
| chr11:76497480
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0002g0264 | 2 | HG01433.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1408+1011G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497480 | ||||||
| chr11:76497503
|
T | A | 6 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+1034T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497503 | ||||||
| chr11:76497612
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1408+1143G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497612 | ||||||
| chr11:76497626
|
G | T | 1 | a0001c0001t0004g0098 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1408+1157G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497626 | ||||||
| chr11:76497853
|
C | G | 1 | a0001c0002t0001g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1408+1384C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76497853 | ||||||
| chr11:76498049
|
A | G | 1 | a0004c0007t0002g0121 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1408+1580A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76498049 | ||||||
| chr11:76498409
|
A | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+1940A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76498409 | ||||||
| chr11:76498424
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1408+1955T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76498424 | ||||||
| chr11:76498573
|
A | G | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1408+2104A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76498573 | ||||||
| chr11:76498608
|
A | AT | 25 | a0001c0001t0002g0139a0001c0001t0002g0161a0001c0001t0002g0255others(22): Show | 26 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1408+2147dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76498608 | |||||
| chr11:76498973
|
T | C | 4 | a0001c0001t0003g0201a0002c0005t0003g0197a0002c0005t0003g0198others(1): Show | 4 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+2504T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76498973 | ||||||
| chr11:76499026
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1408+2557A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499026 | ||||||
| chr11:76499118
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0002g0283 | 2 | HG00140.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1408+2649C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499118 | ||||||
| chr11:76499153
|
G | T | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1408+2684G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499153 | ||||||
| chr11:76499204
|
G | T | 1 | a0001c0002t0001g0041 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1408+2735G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499204 | ||||||
| chr11:76499275
|
C | CT | 47 | a0001c0001t0001g0291a0001c0001t0001g0308a0001c0001t0002g0093others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1408+2836dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499275
|
C | CTT | 21 | a0001c0001t0001g0003a0001c0001t0001g0292a0001c0001t0001g0293others(18): Show | 22 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408+2835_1408+283 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499275
|
CT | C | 34 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1408+2836delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499275
|
CTT | C | 82 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(79): Show | 82 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1408+2835_1408+283 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499275
|
CTTT | C | 10 | a0001c0001t0001g0343a0001c0001t0026g0354a0001c0002t0001g0027others(7): Show | 10 | HG00323.hp1 HG02155.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1408+2834_1408+283 others(7): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499275
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0156 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1408+2825_1408+283 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76499275 | |||||
| chr11:76499313
|
A | C | 1 | a0001c0001t0002g0114 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1408+2844A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499313 | ||||||
| chr11:76499332
|
G | T | 30 | a0001c0001t0002g0004a0001c0001t0002g0139a0001c0001t0002g0161others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1408+2863G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499332 | ||||||
| chr11:76499356
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1408+2887C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499356 | ||||||
| chr11:76499448
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1408+2979C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499448 | ||||||
| chr11:76499578
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3109C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499578 | ||||||
| chr11:76499733
|
G | A | 2 | a0001c0001t0002g0255a0001c0001t0002g0260 | 2 | HG00280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1408+3264G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499733 | ||||||
| chr11:76499798
|
G | A | 5 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01192.hp2 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+3329G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499798 | ||||||
| chr11:76499885
|
C | T | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1408+3416C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499885 | ||||||
| chr11:76499998
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1408+3529G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76499998 | ||||||
| chr11:76500018
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1408+3549A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500018 | ||||||
| chr11:76500050
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1408+3581G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500050 | ||||||
| chr11:76500076
|
C | CA | 8 | a0001c0001t0001g0304a0001c0001t0006g0010a0001c0002t0001g0030others(5): Show | 8 | HG00609.hp1 HG02027.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408+3623dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76500076 | |||||
| chr11:76500076
|
CA | C | 205 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1408+3623delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76500076 | |||||
| chr11:76500098
|
C | T | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(2): Show | 5 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+3629C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500098 | ||||||
| chr11:76500377
|
G | A | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1408+3908G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500377 | ||||||
| chr11:76500607
|
T | C | 1 | a0001c0003t0001g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408+4138T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500607 | ||||||
| chr11:76500658
|
A | G | 1 | a0001c0001t0006g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1408+4189A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500658 | ||||||
| chr11:76500897
|
C | T | 11 | a0001c0001t0002g0139a0001c0001t0002g0257a0001c0001t0002g0258others(8): Show | 11 | HG00733.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408+4428C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76500897 | ||||||
| chr11:76501120
|
T | C | 71 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(68): Show | 71 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1408+4651T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76501120 | ||||||
| chr11:76501162
|
C | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1408+4693C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76501162 | ||||||
| chr11:76501308
|
A | G | 1 | a0001c0001t0015g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1408+4839A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76501308 | ||||||
| chr11:76501675
|
T | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1408+5206T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76501675 | ||||||
| chr11:76502044
|
G | GA | 13 | a0001c0001t0001g0308a0001c0001t0001g0316a0001c0001t0001g0317others(10): Show | 13 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408+5593dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502044 | |||||
| chr11:76502044
|
GA | G | 90 | a0001c0001t0001g0298a0001c0001t0001g0323a0001c0001t0001g0330others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1408+5593delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502044 | |||||
| chr11:76502287
|
C | CA | 148 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0322others(145): Show | 148 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1408+5842dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502287 | |||||
| chr11:76502287
|
C | CAA | 30 | a0001c0001t0001g0318a0001c0001t0001g0326a0001c0001t0001g0332others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1408+5841_1408+584 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502287 | |||||
| chr11:76502287
|
CA | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(25): Show | 29 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1408+5842delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502287 | |||||
| chr11:76502312
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1408+5843G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502312 | ||||||
| chr11:76502466
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1408+5997G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502466 | ||||||
| chr11:76502510
|
C | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1408+6041C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502510 | ||||||
| chr11:76502530
|
T | TA | 12 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG00323.hp2 HG00597.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1408+6070dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76502530 | |||||
| chr11:76502538
|
A | C | 1 | a0001c0002t0023g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1408+6069A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502538 | ||||||
| chr11:76502601
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1408+6132G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502601 | ||||||
| chr11:76502697
|
A | C | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG00544.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1408+6228A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502697 | ||||||
| chr11:76502913
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1408+6444C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502913 | ||||||
| chr11:76502965
|
A | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1408+6496A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76502965 | ||||||
| chr11:76503023
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1408+6554C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503023 | ||||||
| chr11:76503041
|
C | T | 12 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG00323.hp2 HG00597.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1408+6572C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503041 | ||||||
| chr11:76503098
|
C | T | 1 | a0001c0001t0015g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1408+6629C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503098 | ||||||
| chr11:76503099
|
G | A | 1 | a0001c0001t0012g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1408+6630G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503099 | ||||||
| chr11:76503128
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1408+6659C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503128 | ||||||
| chr11:76503232
|
C | T | 1 | a0001c0002t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1408+6763C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503232 | ||||||
| chr11:76503300
|
C | CA | 206 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(203): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1408+6854dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76503300 | |||||
| chr11:76503300
|
C | CAA | 16 | a0001c0001t0001g0293a0001c0001t0001g0302a0001c0001t0001g0318others(13): Show | 16 | HG00544.hp2 HG00642.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1408+6853_1408+685 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76503300 | |||||
| chr11:76503300
|
CA | C | 10 | a0001c0001t0002g0008a0001c0001t0002g0092a0001c0001t0002g0115others(7): Show | 10 | HG02074.hp1 HG03491.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+6854delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76503300 | |||||
| chr11:76503318
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+6849A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503318 | ||||||
| chr11:76503321
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+6852A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503321 | ||||||
| chr11:76503371
|
A | G | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1408+6902A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503371 | ||||||
| chr11:76503396
|
A | G | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1408+6927A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503396 | ||||||
| chr11:76503403
|
C | T | 2 | a0001c0001t0002g0178a0001c0002t0001g0035 | 2 | HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1408+6934C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503403 | ||||||
| chr11:76503468
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0300 | 2 | NA18947.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1408+6999G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503468 | ||||||
| chr11:76503478
|
T | A | 3 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | NA18979.hp1 NA19001.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1408+7009T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503478 | ||||||
| chr11:76503551
|
A | G | 1 | a0001c0001t0001g0334 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1408+7082A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503551 | ||||||
| chr11:76503889
|
A | G | 12 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG00323.hp2 HG00597.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1408+7420A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503889 | ||||||
| chr11:76503909
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1408+7440C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503909 | ||||||
| chr11:76503930
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1408+7461G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503930 | ||||||
| chr11:76503931
|
C | T | 1 | a0001c0001t0003g0238 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1408+7462C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76503931 | ||||||
| chr11:76503951
|
A | AT | 7 | a0001c0001t0001g0315a0001c0001t0001g0323a0001c0001t0001g0324others(4): Show | 7 | HG02055.hp1 HG03209.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1408+7497dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76503951 | |||||
| chr11:76504442
|
A | G | 3 | a0001c0001t0004g0101a0001c0001t0004g0102a0001c0001t0004g0103 | 3 | NA18997.hp1 NA19085.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1408+7973A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504442 | ||||||
| chr11:76504492
|
A | G | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1408+8023A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504492 | ||||||
| chr11:76504522
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1408+8053A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504522 | ||||||
| chr11:76504541
|
T | C | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA18974.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1408+8072T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504541 | ||||||
| chr11:76504570
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1408+8101A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504570 | ||||||
| chr11:76504612
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02717.hp2 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1408+8143C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504612 | ||||||
| chr11:76504764
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1408+8295C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504764 | ||||||
| chr11:76504932
|
A | G | 1 | a0001c0002t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1409-8454A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504932 | ||||||
| chr11:76504947
|
T | G | 324 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1409-8439T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76504947 | ||||||
| chr11:76505057
|
A | G | 11 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(8): Show | 11 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.1409-8329A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505057 | ||||||
| chr11:76505201
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-8185C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505201 | ||||||
| chr11:76505221
|
T | C | 326 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1409-8165T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505221 | ||||||
| chr11:76505234
|
A | G | 2 | a0001c0001t0006g0010a0001c0001t0006g0011 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1409-8152A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505234 | ||||||
| chr11:76505281
|
C | T | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1409-8105C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505281 | ||||||
| chr11:76505343
|
G | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02717.hp2 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1409-8043G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505343 | ||||||
| chr11:76505362
|
A | AT | 110 | a0001c0001t0001g0003a0001c0001t0001g0292a0001c0001t0001g0293others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1409-8005dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76505362 | |||||
| chr11:76505362
|
A | ATT | 114 | a0001c0001t0001g0291a0001c0001t0001g0294a0001c0001t0001g0302others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1409-8006_1409-800 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76505362 | |||||
| chr11:76505362
|
A | ATTT | 22 | a0001c0001t0002g0093a0001c0001t0002g0106a0001c0001t0002g0117others(19): Show | 22 | HG00733.hp2 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1409-8007_1409-800 others(7): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76505362 | |||||
| chr11:76505402
|
T | C | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1409-7984T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505402 | ||||||
| chr11:76505576
|
G | A | 5 | a0001c0001t0003g0232a0001c0001t0014g0287a0001c0001t0014g0288others(2): Show | 5 | HG02572.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-7810G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505576 | ||||||
| chr11:76505628
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1409-7758C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505628 | ||||||
| chr11:76505639
|
C | T | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1409-7747C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505639 | ||||||
| chr11:76505829
|
C | T | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1409-7557C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505829 | ||||||
| chr11:76505844
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1409-7542G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505844 | ||||||
| chr11:76505922
|
G | A | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1409-7464G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76505922 | ||||||
| chr11:76506067
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1409-7319G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506067 | ||||||
| chr11:76506090
|
A | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1409-7296A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506090 | ||||||
| chr11:76506161
|
G | A | 1 | a0001c0001t0004g0289 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1409-7225G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506161 | ||||||
| chr11:76506180
|
A | T | 10 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.1409-7206A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506180 | ||||||
| chr11:76506214
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1409-7172A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506214 | ||||||
| chr11:76506215
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1409-7171G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506215 | ||||||
| chr11:76506299
|
C | A | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1409-7087C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506299 | ||||||
| chr11:76506420
|
A | G | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1409-6966A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506420 | ||||||
| chr11:76506500
|
C | T | 209 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1409-6886C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506500 | ||||||
| chr11:76506669
|
C | T | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1409-6717C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506669 | ||||||
| chr11:76506776
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-6610C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506776 | ||||||
| chr11:76506777
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1409-6609G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506777 | ||||||
| chr11:76506860
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1409-6526A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76506860 | ||||||
| chr11:76507546
|
T | G | 38 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(35): Show | 38 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1409-5840T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76507546 | ||||||
| chr11:76507837
|
AT | A | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1409-5540delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76507837 | |||||
| chr11:76507853
|
CTTTTTCT others(6): Show |
C | 1 | a0001c0002t0001g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1409-5527_1409-551 others(17): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76507853 | |||||
| chr11:76507859
|
CTTTTTCT others(8): Show |
C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1409-5512_1409-549 others(19): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76507859 | |||||
| chr11:76507865
|
CT | C | 282 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1409-5507delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76507865 | |||||
| chr11:76507865
|
CTT | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1409-5508_1409-550 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76507865 | |||||
| chr11:76507879
|
T | C | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1409-5507T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76507879 | ||||||
| chr11:76507880
|
C | T | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1409-5506C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76507880 | ||||||
| chr11:76508039
|
T | A | 15 | a0001c0001t0002g0282a0001c0001t0004g0095a0001c0001t0004g0096others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1409-5347T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508039 | ||||||
| chr11:76508064
|
T | G | 1 | a0001c0001t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1409-5322T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508064 | ||||||
| chr11:76508110
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1409-5276A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508110 | ||||||
| chr11:76508113
|
C | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1409-5273C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508113 | ||||||
| chr11:76508291
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1409-5095C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508291 | ||||||
| chr11:76508327
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1409-5059A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508327 | ||||||
| chr11:76508343
|
C | CT | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1409-5030dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76508343 | |||||
| chr11:76508443
|
C | G | 1 | a0001c0001t0016g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1409-4943C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508443 | ||||||
| chr11:76508444
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1409-4942A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508444 | ||||||
| chr11:76508482
|
T | C | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1409-4904T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508482 | ||||||
| chr11:76508662
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1409-4724T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508662 | ||||||
| chr11:76508663
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1409-4723A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508663 | ||||||
| chr11:76508665
|
A | G | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1409-4721A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508665 | ||||||
| chr11:76508788
|
A | G | 1 | a0001c0001t0003g0321 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1409-4598A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508788 | ||||||
| chr11:76508906
|
G | C | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1409-4480G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508906 | ||||||
| chr11:76508946
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1409-4440G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508946 | ||||||
| chr11:76508972
|
C | T | 1 | a0001c0001t0002g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1409-4414C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508972 | ||||||
| chr11:76508987
|
G | T | 1 | a0001c0003t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1409-4399G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76508987 | ||||||
| chr11:76509054
|
A | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-4332A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509054 | ||||||
| chr11:76509233
|
A | G | 2 | a0001c0001t0011g0082a0001c0001t0016g0091 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1409-4153A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509233 | ||||||
| chr11:76509302
|
G | A | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1409-4084G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509302 | ||||||
| chr11:76509352
|
G | A | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1409-4034G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509352 | ||||||
| chr11:76509443
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1409-3943A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509443 | ||||||
| chr11:76509488
|
G | A | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-3898G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509488 | ||||||
| chr11:76509784
|
C | G | 1 | a0001c0002t0001g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1409-3602C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509784 | ||||||
| chr11:76509815
|
G | A | 1 | a0001c0001t0027g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1409-3571G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76509815 | ||||||
| chr11:76510044
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1409-3342G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510044 | ||||||
| chr11:76510168
|
A | C | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1409-3218A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510168 | ||||||
| chr11:76510301
|
G | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1409-3085G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510301 | ||||||
| chr11:76510453
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1409-2933G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510453 | ||||||
| chr11:76510672
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1409-2714G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510672 | ||||||
| chr11:76510774
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1409-2612T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510774 | ||||||
| chr11:76510787
|
A | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1409-2599A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510787 | ||||||
| chr11:76510902
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1409-2484G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510902 | ||||||
| chr11:76510906
|
A | T | 1 | a0001c0002t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1409-2480A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510906 | ||||||
| chr11:76510907
|
A | C | 1 | a0001c0002t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1409-2479A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510907 | ||||||
| chr11:76510909
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1409-2477T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510909 | ||||||
| chr11:76510931
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-2455A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510931 | ||||||
| chr11:76510989
|
C | T | 2 | a0001c0001t0011g0082a0001c0001t0016g0091 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1409-2397C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76510989 | ||||||
| chr11:76511064
|
G | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1409-2322G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76511064 | ||||||
| chr11:76511123
|
CT | C | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1409-2258delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76511123 | |||||
| chr11:76511348
|
CTTAA | C | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(2): Show | 5 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-2035_1409-203 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr11 | 76511348 | |||||
| chr11:76511409
|
T | C | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1409-1977T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76511409 | ||||||
| chr11:76511424
|
C | T | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1409-1962C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76511424 | ||||||
| chr11:76511765
|
T | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0012 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1409-1621T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76511765 | ||||||
| chr11:76512256
|
T | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1409-1130T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76512256 | ||||||
| chr11:76512278
|
G | A | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1409-1108G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76512278 | ||||||
| chr11:76512651
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1409-735G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76512651 | ||||||
| chr11:76513179
|
A | G | 2 | a0001c0001t0007g0126a0001c0001t0018g0084 | 2 | HG02273.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1409-207A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 10/21 | chr11 | 76513179 | ||||||
| chr11:76513572
|
T | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558+37T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76513572 | ||||||
| chr11:76513930
|
C | A | 1 | a0001c0001t0002g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1558+395C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76513930 | ||||||
| chr11:76513985
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1558+450A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76513985 | ||||||
| chr11:76514213
|
C | T | 2 | a0001c0002t0001g0038a0001c0002t0001g0047 | 2 | HG00438.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1558+678C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514213 | ||||||
| chr11:76514257
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0002g0177 | 2 | HG04199.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1558+722C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514257 | ||||||
| chr11:76514614
|
T | C | 3 | a0001c0001t0002g0254a0001c0001t0002g0279a0001c0001t0002g0280 | 3 | HG02886.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1558+1079T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514614 | ||||||
| chr11:76514622
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+1087T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514622 | ||||||
| chr11:76514698
|
G | A | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558+1163G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514698 | ||||||
| chr11:76514748
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1558+1213C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76514748 | ||||||
| chr11:76515044
|
G | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1559-1098G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515044 | ||||||
| chr11:76515072
|
GT | G | 16 | a0001c0001t0002g0214a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-1056delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 76515072 | |||||
| chr11:76515142
|
G | C | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1559-1000G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515142 | ||||||
| chr11:76515206
|
T | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1559-936T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515206 | ||||||
| chr11:76515206
|
T | TG | 28 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(25): Show | 29 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1559-926dupG | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 76515206 | |||||
| chr11:76515206
|
TG | T | 118 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(115): Show | 118 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1559-926delG | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 76515206 | |||||
| chr11:76515208
|
G | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0020 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1559-934G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515208 | ||||||
| chr11:76515211
|
G | A | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-931G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515211 | ||||||
| chr11:76515217
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1559-925A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515217 | ||||||
| chr11:76515357
|
G | A | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1559-785G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515357 | ||||||
| chr11:76515513
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1559-629G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515513 | ||||||
| chr11:76515542
|
T | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1559-600T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76515542 | ||||||
| chr11:76516069
|
A | G | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1559-73A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76516069 | ||||||
| chr11:76516080
|
A | G | 1 | a0001c0001t0007g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1559-62A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76516080 | ||||||
| chr11:76516138
|
G | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
splice_region_variant&intron_variant | LOW | c.1559-4G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 11/21 | chr11 | 76516138 | ||||||
| chr11:76516480
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1729+168T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76516480 | ||||||
| chr11:76516551
|
G | A | 10 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(7): Show | 10 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1729+239G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76516551 | ||||||
| chr11:76516915
|
G | A | 1 | a0001c0002t0010g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1729+603G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76516915 | ||||||
| chr11:76517213
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1729+901G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517213 | ||||||
| chr11:76517213
|
G | T | 319 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1729+901G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517213 | ||||||
| chr11:76517214
|
A | T | 1 | a0001c0001t0002g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1729+902A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517214 | ||||||
| chr11:76517281
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1729+969C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517281 | ||||||
| chr11:76517497
|
T | G | 196 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1729+1185T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517497 | ||||||
| chr11:76517537
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1729+1225T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517537 | ||||||
| chr11:76517641
|
G | A | 3 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0265 | 3 | HG01168.hp1 HG01169.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1729+1329G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517641 | ||||||
| chr11:76517804
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1729+1492C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517804 | ||||||
| chr11:76517817
|
ACTTGGCA others(5): Show |
A | 1 | a0001c0001t0002g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1729+1506_1729+151 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517817 | ||||||
| chr11:76517822
|
GCATACAG others(6): Show |
G | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1729+1526_1729+153 others(17): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76517822 | |||||
| chr11:76517878
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1729+1566T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517878 | ||||||
| chr11:76517947
|
T | C | 33 | a0001c0001t0002g0004a0001c0001t0002g0139a0001c0001t0002g0161others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.1729+1635T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76517947 | ||||||
| chr11:76518116
|
C | T | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729+1804C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518116 | ||||||
| chr11:76518167
|
C | CT | 12 | a0001c0001t0001g0291a0001c0001t0001g0323a0001c0001t0001g0324others(9): Show | 12 | HG01433.hp2 HG02895.hp1 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.1729+1875dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518167 | |||||
| chr11:76518167
|
C | CTT | 114 | a0001c0001t0002g0008a0001c0001t0002g0089a0001c0001t0002g0092others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1729+1874_1729+187 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518167 | |||||
| chr11:76518173
|
T | C | 2 | a0001c0002t0001g0038a0001c0002t0001g0047 | 2 | HG00438.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1729+1861T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518173 | ||||||
| chr11:76518241
|
T | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1729+1929T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518241 | ||||||
| chr11:76518255
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1729+1943C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518255 | ||||||
| chr11:76518516
|
T | A | 311 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1729+2204T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518516 | ||||||
| chr11:76518625
|
T | A | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+2313T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518625 | ||||||
| chr11:76518653
|
T | C | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729+2341T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518653 | ||||||
| chr11:76518678
|
T | C | 73 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1729+2366T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518678 | ||||||
| chr11:76518684
|
C | CAT | 6 | a0001c0001t0001g0322a0001c0001t0014g0287a0001c0001t0014g0288others(3): Show | 6 | HG01175.hp2 HG01346.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729+2391_1729+239 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATAT | 21 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1729+2389_1729+239 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATATATA others(1): Show |
18 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0123others(15): Show | 18 | HG01175.hp1 HG01952.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.1729+2385_1729+239 others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATATATA others(3): Show |
8 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0269others(5): Show | 8 | HG01071.hp2 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1729+2383_1729+239 others(14): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATATATA others(5): Show |
11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG00280.hp2 HG00733.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729+2381_1729+239 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATATATA others(7): Show |
4 | a0001c0001t0002g0161a0001c0001t0002g0264a0001c0001t0002g0267others(1): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729+2379_1729+239 others(18): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
C | CATATATA others(15): Show |
3 | a0001c0001t0002g0004a0001c0001t0002g0261a0001c0001t0002g0283 | 3 | HG00140.hp1 HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(26): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518684
|
CAT | C | 7 | a0001c0001t0001g0332a0001c0001t0004g0098a0001c0001t0004g0099others(4): Show | 7 | HG01106.hp2 NA18970.hp2 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.1729+2391_1729+239 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518684 | |||||
| chr11:76518702
|
TA | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0296a0001c0001t0011g0082 | 3 | HG02080.hp2 HG02451.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1729+2391delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518702 | ||||||
| chr11:76518703
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1729+2392_1729+239 others(23): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0139a0001c0001t0002g0274a0001c0001t0002g0276 | 3 | HG01243.hp1 HG01496.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0002g0127a0001c0001t0002g0177a0001c0001t0002g0254others(2): Show | 5 | HG02622.hp2 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(14): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1729+2392_1729+239 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATAT others(1): Show |
39 | a0001c0001t0002g0008a0001c0001t0002g0093a0001c0001t0002g0106others(36): Show | 39 | HG00408.hp2 HG01099.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATAT others(3): Show |
4 | a0001c0001t0002g0120a0001c0001t0002g0140a0001c0001t0002g0272others(1): Show | 4 | HG02615.hp1 HG04184.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(14): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATATTT others(1): Show |
11 | a0001c0001t0002g0105a0001c0001t0002g0113a0001c0001t0002g0116others(8): Show | 11 | HG01192.hp2 HG01993.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATATT | 39 | a0001c0001t0002g0205a0001c0001t0002g0214a0001c0001t0003g0081others(36): Show | 39 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | ATTTT | 8 | a0001c0001t0002g0210a0001c0001t0003g0230a0001c0001t0005g0213others(5): Show | 8 | HG00621.hp2 HG00642.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1729+2398_1729+240 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518703
|
A | T | 8 | a0001c0001t0003g0236a0001c0001t0016g0091a0001c0002t0001g0031others(5): Show | 8 | HG01515.hp2 HG02040.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1729+2391A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518703 | ||||||
| chr11:76518703
|
AT | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(28): Show | 32 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1729+2401delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518703 | |||||
| chr11:76518704
|
T | TA | 3 | a0001c0001t0001g0308a0001c0002t0001g0054a0001c0003t0001g0247 | 3 | HG02257.hp1 HG02647.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1729+2392_1729+239 others(5): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518704 | ||||||
| chr11:76518705
|
T | A | 33 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1729+2393T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518705 | ||||||
| chr11:76518706
|
T | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(9): Show | 13 | HG00544.hp2 NA18747.hp1 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.1729+2394T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518706 | ||||||
| chr11:76518707
|
T | A | 5 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 5 | HG00140.hp1 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1729+2395T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518707 | ||||||
| chr11:76518708
|
T | A | 1 | a0001c0001t0001g0003 | 2 | NA18969.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1729+2396T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518708 | ||||||
| chr11:76518745
|
G | A | 16 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(13): Show | 16 | HG00438.hp1 HG00735.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1729+2433G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518745 | ||||||
| chr11:76518827
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1729+2515G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76518827 | ||||||
| chr11:76518858
|
T | TTG | 189 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(186): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1729+2570_1729+257 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518858 | |||||
| chr11:76518858
|
T | TTGTG | 18 | a0001c0001t0002g0167a0001c0001t0002g0170a0001c0001t0002g0357others(15): Show | 18 | HG00323.hp2 HG00597.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.1729+2568_1729+257 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518858 | |||||
| chr11:76518858
|
T | TTGTGTG | 73 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1729+2566_1729+257 others(10): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518858 | |||||
| chr11:76518858
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1729+2560_1729+257 others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76518858 | |||||
| chr11:76519065
|
CT | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(26): Show | 30 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1729+2770delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76519065 | |||||
| chr11:76519210
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1729+2898G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519210 | ||||||
| chr11:76519254
|
A | G | 1 | a0001c0001t0001g0333 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1729+2942A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519254 | ||||||
| chr11:76519313
|
C | A | 196 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1729+3001C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519313 | ||||||
| chr11:76519357
|
A | G | 354 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1729+3045A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519357 | ||||||
| chr11:76519661
|
G | A | 1 | a0001c0001t0009g0277 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1729+3349G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519661 | ||||||
| chr11:76519782
|
A | G | 2 | a0001c0001t0003g0285a0001c0001t0003g0286 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1730-3373A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519782 | ||||||
| chr11:76519844
|
C | T | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1730-3311C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519844 | ||||||
| chr11:76519949
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1730-3206T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76519949 | ||||||
| chr11:76520183
|
A | G | 73 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1730-2972A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76520183 | ||||||
| chr11:76520776
|
T | G | 5 | a0001c0001t0003g0186a0001c0001t0003g0196a0001c0001t0003g0204others(2): Show | 5 | NA18939.hp1 NA18951.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1730-2379T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76520776 | ||||||
| chr11:76520779
|
C | T | 5 | a0001c0001t0003g0186a0001c0001t0003g0196a0001c0001t0003g0204others(2): Show | 5 | NA18939.hp1 NA18951.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1730-2376C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76520779 | ||||||
| chr11:76520808
|
TTAAG | T | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1730-2342_1730-233 others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76520808 | |||||
| chr11:76520904
|
A | T | 1 | a0001c0002t0001g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1730-2251A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76520904 | ||||||
| chr11:76521120
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1730-2035A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521120 | ||||||
| chr11:76521180
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1730-1975A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521180 | ||||||
| chr11:76521224
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1730-1931A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521224 | ||||||
| chr11:76521314
|
T | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1730-1841T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521314 | ||||||
| chr11:76521569
|
C | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1730-1586C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521569 | ||||||
| chr11:76521765
|
T | TA | 10 | a0001c0001t0002g0004a0001c0001t0002g0234a0001c0001t0002g0357others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1730-1372dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76521765 | |||||
| chr11:76521765
|
TA | T | 14 | a0001c0001t0002g0008a0001c0001t0002g0131a0001c0001t0002g0280others(11): Show | 14 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1730-1372delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76521765 | |||||
| chr11:76521766
|
A | T | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1730-1389A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521766 | ||||||
| chr11:76521787
|
C | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1730-1368C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76521787 | ||||||
| chr11:76522352
|
CT | C | 86 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1730-773delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76522352 | |||||
| chr11:76522352
|
CTT | C | 126 | a0001c0001t0001g0294a0001c0001t0001g0311a0001c0001t0002g0008others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1730-774_1730-773d others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76522352 | |||||
| chr11:76522352
|
CTTT | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(94): Show | 98 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1730-775_1730-773d others(5): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76522352 | |||||
| chr11:76522352
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1730-786_1730-773d others(16): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 76522352 | |||||
| chr11:76522391
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1730-764C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522391 | ||||||
| chr11:76522392
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1730-763G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522392 | ||||||
| chr11:76522428
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1730-727C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522428 | ||||||
| chr11:76522441
|
C | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1730-714C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522441 | ||||||
| chr11:76522517
|
G | A | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1730-638G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522517 | ||||||
| chr11:76522608
|
G | T | 1 | a0001c0001t0007g0129 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1730-547G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522608 | ||||||
| chr11:76522610
|
G | A | 210 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1730-545G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522610 | ||||||
| chr11:76522660
|
C | G | 1 | a0001c0003t0001g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1730-495C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522660 | ||||||
| chr11:76522724
|
A | C | 1 | a0001c0001t0002g0263 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1730-431A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522724 | ||||||
| chr11:76522795
|
A | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730-360A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522795 | ||||||
| chr11:76522799
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1730-356A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522799 | ||||||
| chr11:76522960
|
G | A | 324 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1730-195G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76522960 | ||||||
| chr11:76523141
|
C | T | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1730-14C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 12/21 | chr11 | 76523141 | ||||||
| chr11:76523424
|
C | T | 1 | a0001c0001t0002g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1866+133C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523424 | ||||||
| chr11:76523484
|
T | C | 210 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1866+193T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523484 | ||||||
| chr11:76523540
|
C | G | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1866+249C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523540 | ||||||
| chr11:76523655
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1866+364G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523655 | ||||||
| chr11:76523704
|
C | CT | 19 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(16): Show | 19 | HG00741.hp2 HG01192.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1866+434dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTT | 9 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(6): Show | 9 | HG00323.hp2 HG00597.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1866+433_1866+434d others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTT | 55 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0322others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1866+431_1866+434d others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTTT | 46 | a0001c0001t0001g0340a0001c0001t0001g0350a0001c0001t0026g0354others(43): Show | 46 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1866+430_1866+434d others(7): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTTTT | 24 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(21): Show | 25 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1866+429_1866+434d others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTTTTT | 6 | a0001c0001t0001g0300a0001c0002t0001g0052a0001c0002t0001g0053others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1866+428_1866+434d others(9): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0006g0009a0001c0001t0006g0012 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1866+425_1866+434d others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523704
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0013 | 3 | HG02055.hp2 HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1866+424_1866+434d others(13): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76523704 | |||||
| chr11:76523824
|
C | T | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1866+533C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523824 | ||||||
| chr11:76523909
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1866+618A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76523909 | ||||||
| chr11:76524208
|
G | A | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1866+917G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524208 | ||||||
| chr11:76524244
|
T | G | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1866+953T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524244 | ||||||
| chr11:76524397
|
T | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1866+1106T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524397 | ||||||
| chr11:76524469
|
T | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1866+1178T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524469 | ||||||
| chr11:76524472
|
G | A | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1866+1181G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524472 | ||||||
| chr11:76524535
|
ATTCAGAT others(1): Show |
A | 15 | a0001c0001t0002g0173a0001c0001t0004g0095a0001c0001t0004g0096others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1866+1251_1866+125 others(12): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76524535 | |||||
| chr11:76524620
|
C | G | 3 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273 | 3 | NA18979.hp1 NA19001.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1866+1329C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524620 | ||||||
| chr11:76524653
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1866+1362T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524653 | ||||||
| chr11:76524740
|
T | A | 1 | a0001c0002t0001g0035 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1866+1449T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524740 | ||||||
| chr11:76524900
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1867-1562C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76524900 | ||||||
| chr11:76525057
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1867-1405A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525057 | ||||||
| chr11:76525176
|
A | G | 73 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1867-1286A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525176 | ||||||
| chr11:76525279
|
A | T | 1 | a0001c0001t0005g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1867-1183A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525279 | ||||||
| chr11:76525354
|
T | A | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1867-1108T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525354 | ||||||
| chr11:76525577
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1867-885T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525577 | ||||||
| chr11:76525600
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1867-862A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525600 | ||||||
| chr11:76525704
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1867-758T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525704 | ||||||
| chr11:76525706
|
T | G | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1867-756T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525706 | ||||||
| chr11:76525940
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1867-522A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76525940 | ||||||
| chr11:76526108
|
T | TA | 12 | a0001c0001t0002g0173a0001c0001t0004g0095a0001c0001t0004g0096others(9): Show | 12 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.1867-353dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 76526108 | |||||
| chr11:76526311
|
G | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1867-151G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76526311 | ||||||
| chr11:76526318
|
G | A | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1867-144G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 13/21 | chr11 | 76526318 | ||||||
| chr11:76526643
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.2040+8A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76526643 | ||||||
| chr11:76526681
|
CA | C | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2040+48delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 76526681 | |||||
| chr11:76526775
|
A | G | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2040+140A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76526775 | ||||||
| chr11:76527220
|
C | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2040+585C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527220 | ||||||
| chr11:76527229
|
A | AATGCC | 16 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(13): Show | 16 | HG00323.hp1 HG02015.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.2040+597_2040+601d others(7): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr11 | 76527229 | |||||
| chr11:76527266
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2040+631A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527266 | ||||||
| chr11:76527768
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2041-500G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527768 | ||||||
| chr11:76527870
|
G | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2041-398G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527870 | ||||||
| chr11:76527904
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2041-364C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527904 | ||||||
| chr11:76527943
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2041-325C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76527943 | ||||||
| chr11:76528104
|
G | A | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2041-164G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76528104 | ||||||
| chr11:76528106
|
C | T | 209 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2041-162C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76528106 | ||||||
| chr11:76528116
|
A | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2041-152A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76528116 | ||||||
| chr11:76528151
|
G | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041-117G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 14/21 | chr11 | 76528151 | ||||||
| chr11:76528585
|
C | CT | 40 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(37): Show | 40 | HG00609.hp2 HG01106.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.2239+137dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76528585 | |||||
| chr11:76528585
|
C | CTT | 32 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(29): Show | 33 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.2239+136_2239+137d others(4): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76528585 | |||||
| chr11:76528603
|
T | A | 1 | a0001c0002t0001g0014 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2239+137T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76528603 | ||||||
| chr11:76528744
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2239+278A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76528744 | ||||||
| chr11:76529077
|
G | T | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2239+611G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529077 | ||||||
| chr11:76529106
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2239+640C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529106 | ||||||
| chr11:76529139
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2239+673C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529139 | ||||||
| chr11:76529625
|
C | CA | 11 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(8): Show | 11 | HG00323.hp2 HG00597.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.2239+1167dupA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76529625 | |||||
| chr11:76529642
|
A | G | 1 | a0001c0001t0003g0321 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2239+1176A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529642 | ||||||
| chr11:76529787
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2239+1321G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529787 | ||||||
| chr11:76529905
|
A | T | 1 | a0001c0001t0001g0346 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2239+1439A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529905 | ||||||
| chr11:76529957
|
C | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2239+1491C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76529957 | ||||||
| chr11:76530155
|
G | GT | 118 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(115): Show | 119 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2239+1709dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76530155 | |||||
| chr11:76530155
|
G | GTT | 40 | a0001c0001t0001g0301a0001c0001t0001g0322a0001c0001t0001g0323others(37): Show | 40 | HG00609.hp2 HG01099.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.2239+1708_2239+170 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76530155 | |||||
| chr11:76530206
|
C | T | 1 | a0001c0001t0007g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2239+1740C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530206 | ||||||
| chr11:76530242
|
C | T | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2239+1776C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530242 | ||||||
| chr11:76530269
|
C | G | 3 | a0001c0001t0012g0218a0001c0001t0014g0287a0001c0001t0014g0288 | 3 | HG00639.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2239+1803C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530269 | ||||||
| chr11:76530306
|
C | T | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2239+1840C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530306 | ||||||
| chr11:76530742
|
T | C | 1 | a0001c0001t0025g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2239+2276T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530742 | ||||||
| chr11:76530887
|
T | C | 1 | a0001c0003t0001g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2239+2421T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530887 | ||||||
| chr11:76530958
|
G | A | 2 | a0001c0003t0001g0252a0001c0003t0001g0253 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2239+2492G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76530958 | ||||||
| chr11:76531061
|
C | T | 1 | a0001c0002t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2239+2595C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531061 | ||||||
| chr11:76531063
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2239+2597C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531063 | ||||||
| chr11:76531105
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2239+2639A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531105 | ||||||
| chr11:76531362
|
T | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2239+2896T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531362 | ||||||
| chr11:76531444
|
C | T | 1 | a0001c0001t0026g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2239+2978C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531444 | ||||||
| chr11:76531514
|
A | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2239+3048A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531514 | ||||||
| chr11:76531729
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2239+3263T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76531729 | ||||||
| chr11:76532039
|
C | G | 9 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2239+3573C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532039 | ||||||
| chr11:76532062
|
T | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0304 | 2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2239+3596T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532062 | ||||||
| chr11:76532123
|
G | A | 1 | a0001c0003t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2239+3657G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532123 | ||||||
| chr11:76532260
|
T | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2240-3635T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532260 | ||||||
| chr11:76532351
|
GT | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2240-3528delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76532351 | |||||
| chr11:76532405
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(28): Show | 32 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.2240-3490G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532405 | ||||||
| chr11:76532406
|
T | G | 1 | a0001c0001t0002g0104 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2240-3489T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532406 | ||||||
| chr11:76532418
|
T | C | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2240-3477T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532418 | ||||||
| chr11:76532477
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2240-3418G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532477 | ||||||
| chr11:76532587
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(1): Show | 4 | HG01175.hp2 HG01243.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2240-3308A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532587 | ||||||
| chr11:76532655
|
A | G | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2240-3240A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532655 | ||||||
| chr11:76532857
|
G | A | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2240-3038G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532857 | ||||||
| chr11:76532967
|
T | C | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2240-2928T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76532967 | ||||||
| chr11:76532967
|
TAC | T | 6 | a0001c0001t0002g0104a0001c0001t0005g0086a0001c0001t0005g0110others(3): Show | 6 | HG02074.hp2 NA18949.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2240-2926_2240-292 others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76532967 | |||||
| chr11:76533005
|
A | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2240-2890A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533005 | ||||||
| chr11:76533009
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2240-2886T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533009 | ||||||
| chr11:76533127
|
A | G | 4 | a0001c0001t0002g0157a0001c0001t0002g0160a0001c0001t0002g0169others(1): Show | 4 | HG01975.hp1 HG01993.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2240-2768A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533127 | ||||||
| chr11:76533139
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2240-2756G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533139 | ||||||
| chr11:76533449
|
G | A | 88 | a0001c0001t0002g0008a0001c0001t0002g0089a0001c0001t0002g0092others(85): Show | 88 | HG00408.hp2 HG01099.hp2 HG01175.hp1 others(85): Show |
intron_variant | MODIFIER | c.2240-2446G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533449 | ||||||
| chr11:76533476
|
GT | G | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2240-2418delT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533476 | ||||||
| chr11:76533595
|
T | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2240-2300T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533595 | ||||||
| chr11:76533670
|
C | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2240-2225C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533670 | ||||||
| chr11:76533686
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2240-2209A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533686 | ||||||
| chr11:76533971
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2240-1924G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76533971 | ||||||
| chr11:76534033
|
A | G | 1 | a0001c0001t0003g0321 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2240-1862A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76534033 | ||||||
| chr11:76534302
|
C | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2240-1593C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76534302 | ||||||
| chr11:76534518
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2240-1377G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76534518 | ||||||
| chr11:76534560
|
A | T | 3 | a0001c0001t0002g0254a0001c0001t0002g0279a0001c0001t0002g0280 | 3 | HG02886.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2240-1335A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76534560 | ||||||
| chr11:76534995
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2240-900G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76534995 | ||||||
| chr11:76535006
|
T | G | 1 | a0001c0002t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2240-889T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535006 | ||||||
| chr11:76535101
|
C | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2240-794C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535101 | ||||||
| chr11:76535450
|
A | G | 1 | a0001c0003t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2240-445A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535450 | ||||||
| chr11:76535536
|
A | G | 3 | a0001c0001t0002g0133a0001c0001t0002g0168a0001c0001t0002g0245 | 3 | NA18966.hp1 NA19077.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2240-359A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535536 | ||||||
| chr11:76535660
|
C | G | 3 | a0001c0001t0002g0085a0001c0001t0002g0189a0001c0001t0002g0193 | 3 | NA18943.hp1 NA19010.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2240-235C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535660 | ||||||
| chr11:76535749
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2240-146G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535749 | ||||||
| chr11:76535830
|
G | GT | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2240-52dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr11 | 76535830 | |||||
| chr11:76535830
|
G | T | 1 | a0001c0001t0002g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2240-65G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 15/21 | chr11 | 76535830 | ||||||
| chr11:76536133
|
TTATTATT others(9): Show |
T | 3 | a0001c0001t0001g0298a0001c0001t0001g0301a0001c0001t0001g0312 | 3 | NA18942.hp1 NA18957.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2404+90_2404+105de others(17): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 76536133 | |||||
| chr11:76536276
|
G | A | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2404+217G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76536276 | ||||||
| chr11:76536618
|
A | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(2): Show | 5 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404+559A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76536618 | ||||||
| chr11:76536694
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2404+635A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76536694 | ||||||
| chr11:76536754
|
T | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2404+695T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76536754 | ||||||
| chr11:76537088
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2405-707C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537088 | ||||||
| chr11:76537106
|
A | G | 1 | a0001c0001t0011g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2405-689A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537106 | ||||||
| chr11:76537231
|
T | C | 2 | a0003c0006t0001g0249a0003c0006t0001g0250 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2405-564T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537231 | ||||||
| chr11:76537281
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2405-514G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537281 | ||||||
| chr11:76537578
|
A | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2405-217A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537578 | ||||||
| chr11:76537586
|
C | T | 3 | a0001c0001t0003g0203a0001c0001t0003g0207a0001c0001t0003g0209 | 3 | HG00099.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2405-209C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 16/21 | chr11 | 76537586 | ||||||
| chr11:76537957
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03490.hp2 | splice_region_variant&intron_variant | LOW | c.2560+7G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76537957 | ||||||
| chr11:76538256
|
TTTTG | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2560+322_2560+325d others(6): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr11 | 76538256 | |||||
| chr11:76538322
|
C | T | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2560+372C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76538322 | ||||||
| chr11:76538639
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2560+689C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76538639 | ||||||
| chr11:76538724
|
G | A | 1 | a0001c0001t0001g0351 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2560+774G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76538724 | ||||||
| chr11:76538733
|
A | G | 1 | a0001c0001t0014g0288 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2560+783A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76538733 | ||||||
| chr11:76539037
|
A | G | 6 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0025others(3): Show | 6 | HG01261.hp1 HG01433.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2561-562A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76539037 | ||||||
| chr11:76539330
|
G | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2561-269G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76539330 | ||||||
| chr11:76539376
|
A | T | 1 | a0001c0002t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2561-223A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76539376 | ||||||
| chr11:76539520
|
A | T | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2561-79A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 17/21 | chr11 | 76539520 | ||||||
| chr11:76539704
|
C | A | 1 | a0001c0001t0002g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2602+64C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76539704 | ||||||
| chr11:76539861
|
T | G | 354 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2602+221T>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76539861 | ||||||
| chr11:76540250
|
T | C | 2 | a0001c0003t0001g0247a0001c0003t0001g0248 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2602+610T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76540250 | ||||||
| chr11:76540350
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2602+710A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76540350 | ||||||
| chr11:76540603
|
C | G | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2602+963C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76540603 | ||||||
| chr11:76540733
|
TA | T | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2602+1096delA | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 76540733 | |||||
| chr11:76540774
|
A | G | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2602+1134A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76540774 | ||||||
| chr11:76540942
|
A | C | 1 | a0001c0002t0001g0028 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2603-1274A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76540942 | ||||||
| chr11:76541086
|
C | T | 195 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0085others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2603-1130C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541086 | ||||||
| chr11:76541159
|
G | C | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2603-1057G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541159 | ||||||
| chr11:76541178
|
A | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2603-1038A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541178 | ||||||
| chr11:76541484
|
G | T | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2603-732G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541484 | ||||||
| chr11:76541486
|
T | C | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2603-730T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541486 | ||||||
| chr11:76541587
|
A | G | 80 | a0001c0001t0002g0008a0001c0001t0002g0089a0001c0001t0002g0092others(77): Show | 80 | HG00408.hp2 HG01099.hp2 HG01175.hp1 others(77): Show |
intron_variant | MODIFIER | c.2603-629A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541587 | ||||||
| chr11:76541676
|
T | A | 1 | a0001c0001t0003g0227 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2603-540T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541676 | ||||||
| chr11:76541678
|
G | C | 1 | a0001c0001t0002g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2603-538G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541678 | ||||||
| chr11:76541697
|
G | C | 1 | a0001c0002t0001g0038 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2603-519G>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541697 | ||||||
| chr11:76541920
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2603-296G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 18/21 | chr11 | 76541920 | ||||||
| chr11:76542381
|
T | A | 1 | a0001c0001t0002g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2754+14T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76542381 | ||||||
| chr11:76542745
|
C | CGTTTTTT | 115 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2754+386_2754+392d others(9): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr11 | 76542745 | |||||
| chr11:76542753
|
G | GT | 13 | a0001c0001t0002g0093a0001c0001t0002g0105a0001c0001t0002g0107others(10): Show | 13 | HG01175.hp1 HG01192.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.2754+401dupT | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr11 | 76542753 | |||||
| chr11:76542753
|
G | T | 1 | a0001c0001t0002g0262 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2754+386G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76542753 | ||||||
| chr11:76542754
|
T | TTTTTTG | 37 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(34): Show | 37 | HG00609.hp2 HG01106.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2754+392_2754+393i others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr11 | 76542754 | |||||
| chr11:76542758
|
T | TTGTTTTG | 6 | a0001c0001t0001g0344a0001c0001t0006g0009a0001c0001t0006g0010others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2754+392_2754+393i others(9): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr11 | 76542758 | |||||
| chr11:76543222
|
T | C | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2754+855T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543222 | ||||||
| chr11:76543264
|
C | T | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2754+897C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543264 | ||||||
| chr11:76543316
|
A | G | 357 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2755-943A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543316 | ||||||
| chr11:76543475
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2755-784C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543475 | ||||||
| chr11:76543485
|
C | T | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2755-774C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543485 | ||||||
| chr11:76543495
|
C | T | 72 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0189others(69): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2755-764C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543495 | ||||||
| chr11:76543556
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2755-703C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543556 | ||||||
| chr11:76543585
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2755-674T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543585 | ||||||
| chr11:76543752
|
C | T | 4 | a0001c0001t0002g0157a0001c0001t0002g0160a0001c0001t0002g0169others(1): Show | 4 | HG01975.hp1 HG01993.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2755-507C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543752 | ||||||
| chr11:76543780
|
C | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2755-479C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543780 | ||||||
| chr11:76543827
|
C | T | 2 | a0001c0003t0001g0247a0001c0003t0001g0248 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2755-432C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543827 | ||||||
| chr11:76543878
|
C | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0307 | 2 | HG00544.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2755-381C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543878 | ||||||
| chr11:76543936
|
C | T | 4 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0252others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2755-323C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543936 | ||||||
| chr11:76543945
|
C | G | 122 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0089others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2755-314C>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543945 | ||||||
| chr11:76543979
|
G | A | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2755-280G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76543979 | ||||||
| chr11:76544171
|
T | A | 1 | a0001c0001t0018g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2755-88T>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 19/21 | chr11 | 76544171 | ||||||
| chr11:76544867
|
C | T | 2 | a0001c0001t0013g0118a0001c0001t0013g0320 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3318+45C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76544867 | ||||||
| chr11:76544913
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3318+91T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76544913 | ||||||
| chr11:76545104
|
G | A | 1 | a0001c0001t0011g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3318+282G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545104 | ||||||
| chr11:76545280
|
C | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0352 | 3 | HG01884.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3318+458C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545280 | ||||||
| chr11:76545368
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3319-429G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545368 | ||||||
| chr11:76545561
|
A | G | 2 | a0001c0001t0014g0287a0001c0001t0014g0288 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3319-236A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545561 | ||||||
| chr11:76545603
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3319-194C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545603 | ||||||
| chr11:76545625
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3319-172G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 20/21 | chr11 | 76545625 | ||||||
| chr11:76546338
|
G | A | 1 | a0001c0001t0011g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3819+41G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546338 | ||||||
| chr11:76546409
|
T | C | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3819+112T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546409 | ||||||
| chr11:76546460
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3819+163C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546460 | ||||||
| chr11:76546491
|
A | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(23): Show | 27 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3819+194A>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546491 | ||||||
| chr11:76546519
|
C | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG00140.hp2 HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3819+222C>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546519 | ||||||
| chr11:76546715
|
T | C | 74 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0002g0152others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3819+418T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546715 | ||||||
| chr11:76546795
|
A | G | 7 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0001t0002g0141others(4): Show | 7 | NA18942.hp2 NA18947.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.3819+498A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546795 | ||||||
| chr11:76546884
|
A | G | 14 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3819+587A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546884 | ||||||
| chr11:76546977
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3819+680G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76546977 | ||||||
| chr11:76547481
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3819+1184G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547481 | ||||||
| chr11:76547729
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3819+1432A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547729 | ||||||
| chr11:76547772
|
A | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3819+1475A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547772 | ||||||
| chr11:76547864
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0090 | 2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3819+1567C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547864 | ||||||
| chr11:76547921
|
A | T | 1 | a0001c0001t0003g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3819+1624A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547921 | ||||||
| chr11:76547992
|
G | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 26 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.3819+1695G>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76547992 | ||||||
| chr11:76548108
|
A | T | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3819+1811A>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76548108 | ||||||
| chr11:76548498
|
A | G | 1 | a0001c0001t0002g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3820-1454A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76548498 | ||||||
| chr11:76548750
|
A | G | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3820-1202A>G | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76548750 | ||||||
| chr11:76548848
|
C | T | 2 | a0001c0001t0025g0355a0001c0001t0026g0354 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3820-1104C>T | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76548848 | ||||||
| chr11:76549321
|
T | C | 1 | a0001c0001t0003g0321 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3820-631T>C | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76549321 | ||||||
| chr11:76549497
|
CTACATT | C | 5 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0342others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3820-441_3820-436d others(8): Show |
EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr11 | 76549497 | |||||
| chr11:76549499
|
AC | A | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.3820-452delC | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76549499 | ||||||
| chr11:76549895
|
G | A | 2 | a0001c0002t0001g0066a0001c0002t0001g0077 | 2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.3820-57G>A | EMSY | ENSG00000158636.17 | transcript | ENST00000695367.1 | protein_coding | 21/21 | chr11 | 76549895 |