| geneid | 10771 |
|---|---|
| ensemblid | ENSG00000015171.21 |
| hgncid | 16966 |
| symbol | ZMYND11 |
| name | zinc finger MYND-type containing 11 |
| refseq_nuc | NM_001370100.5 |
| refseq_prot | NP_001357029.1 |
| ensembl_nuc | ENST00000381604.9 |
| ensembl_prot | ENSP00000371017.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 135455 |
| end | 254637 |
| strand | + |
| ver | v1.2 |
| region | chr10:135455-254637 |
| region5000 | chr10:130455-259637 |
| regionname0 | ZMYND11_chr10_135455_254637 |
| regionname5000 | ZMYND11_chr10_130455_259637 |
| 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 | 602 | 342 | 82 | 62 | 146 | 14 | 36 | 110 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1809 | 304 | 70 | 51 | 134 | 14 | 34 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| c0002 | 1/0 | 1809 | 37 | 12 | 11 | 11 | 0 | 2 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| c0003 | 0/0 | 1809 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2292 | 329 | 78 | 58 | 141 | 14 | 36 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0002 | 0/0 | 2292 | 2 | 1 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0003 | 0/0 | 2292 | 2 | 0 | 2 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0004 | 0/0 | 2292 | 2 | 2 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0005 | 0/0 | 2292 | 2 | 0 | 0 | 2 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0006 | 0/0 | 2292 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0007 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0008 | 0/0 | 2292 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0009 | 0/0 | 2292 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| t0010 | 0/0 | 2292 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| 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 | 2 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1809 | 304 | 70 | 51 | 134 | 14 | 34 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0002 | 1/0 | 1809 | 37 | 12 | 11 | 11 | 0 | 2 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0003 | 0/0 | 1809 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4100 | 291 | 66 | 47 | 129 | 14 | 34 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0002 | 0/0 | 4100 | 2 | 1 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0003 | 0/0 | 4100 | 2 | 0 | 2 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0004 | 0/0 | 4100 | 2 | 2 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0005 | 0/0 | 4100 | 2 | 0 | 0 | 2 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0006 | 0/0 | 4100 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0007 | 0/0 | 4100 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0008 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0009 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0001t0010 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0002t0001 | 1/0 | 4100 | 37 | 12 | 11 | 11 | 0 | 2 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| a0001c0003t0001 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | copy fasta | chr10 | 130455 | 259637 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | FIN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0283 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18945 | hp2 | a0001 | c0001 | t0009 | g0319 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | LWK | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ASW | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | GIH | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | USA | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | USA | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0156 | REF | REF | ZMYND11_chr10_130455_259637 | ZMYND11 | chr10 | 130455 | 259637 |
| 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 |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:239488
|
C | T | 1 | a0001c0003 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.660C>T | p.Ala220Ala | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 7/15 | 784/4100 | 660/1809 | 220/602 | chr10 | 239488 | ||
| chr10:249013
|
A | G | 1 | a0001c0001 | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
synonymous_variant | LOW | c.1611A>G | p.Glu537Glu | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/15 | 1735/4100 | 1611/1809 | 537/602 | chr10 | 249013 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:252654
|
G | T | 1 | a0001c0001t0005 | 2 | NA18993.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 184 | chr10 | 252654 | |||||
| chr10:252795
|
G | A | 1 | a0001c0001t0002 | 2 | HG00735.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 325 | chr10 | 252795 | |||||
| chr10:253790
|
T | C | 1 | a0001c0001t0006 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1320T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 1320 | chr10 | 253790 | |||||
| chr10:254315
|
G | A | 1 | a0001c0001t0007 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 1845 | chr10 | 254315 | |||||
| chr10:254338
|
C | A | 1 | a0001c0001t0008 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1868C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 1868 | chr10 | 254338 | |||||
| chr10:254426
|
T | C | 1 | a0001c0001t0009 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1956T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 1956 | chr10 | 254426 | |||||
| chr10:254439
|
G | T | 1 | a0001c0001t0004 | 2 | HG01884.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1969G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 1969 | chr10 | 254439 | |||||
| chr10:254530
|
G | C | 1 | a0001c0001t0003 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2060G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 2060 | chr10 | 254530 | |||||
| chr10:254540
|
A | G | 1 | a0001c0001t0010 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2070A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 15/15 | 2070 | chr10 | 254540 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:135654
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-20+95T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 135654 | ||||||
| chr10:135740
|
G | GGGGCGGG others(21): Show |
1 | a0001c0001t0001g0339 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20+188_-20+215dup others(28): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 135740 | |||||
| chr10:135954
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-20+395G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 135954 | ||||||
| chr10:136160
|
C | T | 75 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(72): Show | 75 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-20+601C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136160 | ||||||
| chr10:136168
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20+609T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136168 | ||||||
| chr10:136196
|
C | G | 27 | a0001c0001t0001g0263a0001c0001t0001g0313a0001c0001t0001g0314others(24): Show | 27 | HG00673.hp2 HG01952.hp1 HG01993.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+637C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136196 | ||||||
| chr10:136206
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-20+647C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136206 | ||||||
| chr10:136242
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-20+683G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136242 | ||||||
| chr10:136359
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-20+800G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136359 | ||||||
| chr10:136390
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20+831C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136390 | ||||||
| chr10:136554
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-20+995C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136554 | ||||||
| chr10:136744
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+1185T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136744 | ||||||
| chr10:136793
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+1234A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136793 | ||||||
| chr10:136961
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20+1402A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136961 | ||||||
| chr10:136995
|
A | G | 13 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-20+1436A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 136995 | ||||||
| chr10:137211
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-20+1652T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 137211 | ||||||
| chr10:137676
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+2117C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 137676 | ||||||
| chr10:137831
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-20+2272G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 137831 | ||||||
| chr10:137985
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+2426T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 137985 | ||||||
| chr10:138110
|
G | GT | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0127others(41): Show | 44 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20+2568dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 138110 | |||||
| chr10:138152
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-20+2593C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 138152 | ||||||
| chr10:138676
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+3117T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 138676 | ||||||
| chr10:138753
|
G | GA | 94 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-20+3206dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 138753 | |||||
| chr10:138782
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+3223C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 138782 | ||||||
| chr10:138882
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+3323C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 138882 | ||||||
| chr10:138971
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+3412T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 138971 | ||||||
| chr10:139013
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+3454C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139013 | ||||||
| chr10:139231
|
G | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+3672G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139231 | ||||||
| chr10:139408
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+3849A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139408 | ||||||
| chr10:139418
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+3859C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139418 | ||||||
| chr10:139518
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-20+3959G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139518 | ||||||
| chr10:139637
|
A | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0134 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-20+4078A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139637 | ||||||
| chr10:139672
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+4113G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139672 | ||||||
| chr10:139704
|
C | CT | 138 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 138 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-20+4169dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 139704 | |||||
| chr10:139704
|
C | CTT | 16 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0132others(13): Show | 16 | HG00558.hp1 HG01255.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+4168_-20+4169d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 139704 | |||||
| chr10:139704
|
C | CTTT | 6 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 6 | HG01358.hp1 HG01496.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+4167_-20+4169d others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 139704 | |||||
| chr10:139704
|
CT | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(38): Show | 43 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-20+4169delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 139704 | |||||
| chr10:139774
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-20+4215C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139774 | ||||||
| chr10:139792
|
A | G | 64 | a0001c0001t0001g0004a0001c0001t0001g0180a0001c0001t0001g0181others(61): Show | 65 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-20+4233A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139792 | ||||||
| chr10:139793
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-20+4234C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139793 | ||||||
| chr10:139868
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-20+4309C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139868 | ||||||
| chr10:139936
|
G | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+4377G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 139936 | ||||||
| chr10:140573
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-20+5014T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 140573 | ||||||
| chr10:140615
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-20+5056T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 140615 | ||||||
| chr10:140740
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-20+5181A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 140740 | ||||||
| chr10:140855
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-20+5296A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 140855 | ||||||
| chr10:140866
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+5307T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 140866 | ||||||
| chr10:141130
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+5571G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 141130 | ||||||
| chr10:141293
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-20+5734A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 141293 | ||||||
| chr10:141625
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-20+6066T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 141625 | ||||||
| chr10:141941
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-20+6382T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 141941 | ||||||
| chr10:141945
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-20+6386A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 141945 | ||||||
| chr10:142024
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20+6465G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142024 | ||||||
| chr10:142046
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+6487G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142046 | ||||||
| chr10:142180
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-20+6621C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142180 | ||||||
| chr10:142344
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-20+6785C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142344 | ||||||
| chr10:142460
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-20+6901C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142460 | ||||||
| chr10:142824
|
A | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+7265A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142824 | ||||||
| chr10:142865
|
A | G | 76 | a0001c0001t0001g0131a0001c0001t0001g0263a0001c0001t0001g0264others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-20+7306A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142865 | ||||||
| chr10:142919
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+7360A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 142919 | ||||||
| chr10:143172
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20+7613T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143172 | ||||||
| chr10:143269
|
C | T | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7710C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143269 | ||||||
| chr10:143284
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+7725G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143284 | ||||||
| chr10:143456
|
G | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0146a0001c0002t0001g0147others(1): Show | 5 | HG02523.hp2 HG02602.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+7897G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143456 | ||||||
| chr10:143475
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-20+7916T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143475 | ||||||
| chr10:143986
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-20+8427A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 143986 | ||||||
| chr10:144007
|
T | TA | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 160 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.-20+8462dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144007 | |||||
| chr10:144007
|
T | TAA | 62 | a0001c0001t0001g0027a0001c0001t0001g0085a0001c0001t0001g0124others(59): Show | 62 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-20+8461_-20+8462d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144007 | |||||
| chr10:144110
|
A | C | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+8551A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144110 | ||||||
| chr10:144151
|
C | G | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+8592C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144151 | ||||||
| chr10:144154
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+8595T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144154 | ||||||
| chr10:144203
|
G | T | 1 | a0001c0002t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-20+8644G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144203 | ||||||
| chr10:144337
|
A | G | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+8778A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144337 | ||||||
| chr10:144364
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0291 | 3 | HG02559.hp1 HG03098.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20+8805G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144364 | ||||||
| chr10:144543
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+8984T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144543 | ||||||
| chr10:144640
|
CT | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-20+9104delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144640 | |||||
| chr10:144640
|
CTT | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-20+9103_-20+9104d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144640 | |||||
| chr10:144640
|
CTTT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0030others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+9102_-20+9104d others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144640 | |||||
| chr10:144692
|
G | GGTTGA | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+9136_-20+9140d others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 144692 | |||||
| chr10:144721
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+9162C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144721 | ||||||
| chr10:144743
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0309 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-20+9184A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144743 | ||||||
| chr10:144744
|
T | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0309 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-20+9185T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144744 | ||||||
| chr10:144754
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0008g0069 | 3 | NA18954.hp1 NA19062.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+9195C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144754 | ||||||
| chr10:144911
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-20+9352T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 144911 | ||||||
| chr10:145089
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-20+9530A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145089 | ||||||
| chr10:145167
|
T | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-20+9608T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145167 | ||||||
| chr10:145198
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-20+9639G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145198 | ||||||
| chr10:145226
|
GTA | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-20+9675_-20+9676d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 145226 | |||||
| chr10:145235
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-20+9676T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145235 | ||||||
| chr10:145262
|
A | G | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+9703A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145262 | ||||||
| chr10:145269
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-20+9710T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145269 | ||||||
| chr10:145320
|
C | T | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+9761C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145320 | ||||||
| chr10:145688
|
A | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-20+10129A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 145688 | ||||||
| chr10:146171
|
C | G | 1 | a0001c0002t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20+10612C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 146171 | ||||||
| chr10:146554
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+10995T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 146554 | ||||||
| chr10:146593
|
C | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-20+11034C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 146593 | ||||||
| chr10:146769
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-20+11210A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 146769 | ||||||
| chr10:146870
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0121 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20+11311G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 146870 | ||||||
| chr10:147279
|
T | G | 1 | a0001c0001t0001g0261 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-20+11720T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 147279 | ||||||
| chr10:147339
|
G | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+11780G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 147339 | ||||||
| chr10:147343
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-20+11784G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 147343 | ||||||
| chr10:147777
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+12218T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 147777 | ||||||
| chr10:147818
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-20+12259C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 147818 | ||||||
| chr10:148211
|
T | TGTCCTAA others(21): Show |
5 | a0001c0001t0001g0138a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG02615.hp2 NA18941.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+12824_-20+1285 others(32): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 148211 | |||||
| chr10:148211
|
TGTCCTAA others(21): Show |
T | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-20+12824_-20+1285 others(32): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 148211 | |||||
| chr10:148211
|
TGTCCTAA others(77): Show |
T | 2 | a0001c0001t0001g0173a0001c0001t0006g0172 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+12768_-20+1285 others(88): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 148211 | |||||
| chr10:148271
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 211 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-20+12712C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148271 | ||||||
| chr10:148275
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20+12716C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148275 | ||||||
| chr10:148299
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+12740C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148299 | ||||||
| chr10:148357
|
A | G | 1 | a0001c0001t0001g0329 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-20+12798A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148357 | ||||||
| chr10:148387
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+12828C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148387 | ||||||
| chr10:148680
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+13121G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148680 | ||||||
| chr10:148826
|
A | G | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-20+13267A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 148826 | ||||||
| chr10:149074
|
TAGGG | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0096others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+13521_-20+1352 others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149074 | |||||
| chr10:149284
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+13725T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149284 | ||||||
| chr10:149285
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0251 | 2 | HG02717.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-20+13726G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149285 | ||||||
| chr10:149285
|
G | GTTA | 99 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(96): Show | 100 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.-20+13765_-20+1376 others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
G | GTTATTA | 52 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(49): Show | 52 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.-20+13762_-20+1376 others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
G | GTTATTAT others(2): Show |
29 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0087others(26): Show | 29 | HG00323.hp2 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-20+13759_-20+1376 others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
G | GTTGTTAT others(2): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0138a0001c0001t0001g0305others(1): Show | 4 | HG00544.hp1 HG00609.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+13728_-20+1372 others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
G | GTTGTTAT others(5): Show |
1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-20+13728_-20+1372 others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
GTTA | G | 19 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 19 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20+13765_-20+1376 others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
GTTATTA | G | 34 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(31): Show | 35 | HG00597.hp1 HG00733.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-20+13762_-20+1376 others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149285
|
GTTATTAT others(2): Show |
G | 66 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-20+13759_-20+1376 others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 149285 | |||||
| chr10:149291
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+13732A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149291 | ||||||
| chr10:149294
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+13735A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149294 | ||||||
| chr10:149328
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-20+13769T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149328 | ||||||
| chr10:149373
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+13814C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149373 | ||||||
| chr10:149762
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+14203A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149762 | ||||||
| chr10:149830
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-20+14271T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149830 | ||||||
| chr10:149989
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+14430C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 149989 | ||||||
| chr10:150024
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-20+14465T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150024 | ||||||
| chr10:150224
|
T | C | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-20+14665T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150224 | ||||||
| chr10:150343
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0083others(16): Show | 20 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+14784G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150343 | ||||||
| chr10:150398
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-20+14839G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150398 | ||||||
| chr10:150403
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-20+14844A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150403 | ||||||
| chr10:150404
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-20+14845G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150404 | ||||||
| chr10:150482
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-20+14923G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150482 | ||||||
| chr10:150691
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0084others(15): Show | 19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+15132G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150691 | ||||||
| chr10:150699
|
A | C | 130 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 130 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-20+15140A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150699 | ||||||
| chr10:150772
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-20+15213G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 150772 | ||||||
| chr10:151227
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+15668C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151227 | ||||||
| chr10:151252
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(217): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+15693C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151252 | ||||||
| chr10:151345
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-20+15786A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151345 | ||||||
| chr10:151504
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-20+15945G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151504 | ||||||
| chr10:151520
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02809.hp1 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-20+15961G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151520 | ||||||
| chr10:151583
|
G | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(61): Show | 65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.-20+16024G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151583 | ||||||
| chr10:151593
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+16034C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151593 | ||||||
| chr10:151594
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20+16035G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151594 | ||||||
| chr10:151626
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+16067G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151626 | ||||||
| chr10:151746
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+16187T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151746 | ||||||
| chr10:151806
|
A | G | 3 | a0001c0002t0001g0153a0001c0002t0001g0171a0001c0002t0001g0179 | 3 | NA18941.hp2 NA18963.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-20+16247A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151806 | ||||||
| chr10:151868
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+16309T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 151868 | ||||||
| chr10:152047
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+16488C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152047 | ||||||
| chr10:152141
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+16582G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152141 | ||||||
| chr10:152466
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-20+16907A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152466 | ||||||
| chr10:152471
|
T | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(217): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-20+16912T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152471 | ||||||
| chr10:152514
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+16955A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152514 | ||||||
| chr10:152532
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-20+16973C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152532 | ||||||
| chr10:152739
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-20+17180C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152739 | ||||||
| chr10:152886
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-20+17327C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 152886 | ||||||
| chr10:153068
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20+17509A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153068 | ||||||
| chr10:153315
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-20+17756T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153315 | ||||||
| chr10:153712
|
G | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+18153G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153712 | ||||||
| chr10:153837
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+18278A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153837 | ||||||
| chr10:153844
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-20+18285G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153844 | ||||||
| chr10:153850
|
C | A | 6 | a0001c0002t0001g0148a0001c0002t0001g0160a0001c0002t0001g0161others(3): Show | 6 | HG01361.hp1 HG01433.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+18291C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 153850 | ||||||
| chr10:154035
|
T | TCACAA | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+18479_-20+1848 others(9): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 154035 | |||||
| chr10:154064
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG00639.hp2 HG03834.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-20+18505G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154064 | ||||||
| chr10:154204
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.-20+18645A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154204 | ||||||
| chr10:154420
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+18861A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154420 | ||||||
| chr10:154503
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-20+18944G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154503 | ||||||
| chr10:154509
|
C | T | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0288others(8): Show | 11 | HG02257.hp1 HG02647.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+18950C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154509 | ||||||
| chr10:154671
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-20+19112G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154671 | ||||||
| chr10:154912
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0130 | 2 | NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-20+19353T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154912 | ||||||
| chr10:154937
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+19378C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154937 | ||||||
| chr10:154938
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-20+19379G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 154938 | ||||||
| chr10:155024
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+19465G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155024 | ||||||
| chr10:155030
|
C | A | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+19471C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155030 | ||||||
| chr10:155054
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-20+19495G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155054 | ||||||
| chr10:155103
|
A | G | 1 | a0001c0001t0007g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-20+19544A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155103 | ||||||
| chr10:155243
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0102others(2): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+19684A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155243 | ||||||
| chr10:155375
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0126 | 3 | NA18978.hp1 NA19002.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-20+19816A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155375 | ||||||
| chr10:155397
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+19838C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155397 | ||||||
| chr10:155604
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-20+20045G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155604 | ||||||
| chr10:155605
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG01123.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-20+20046A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155605 | ||||||
| chr10:155638
|
G | A | 75 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(72): Show | 75 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-20+20079G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155638 | ||||||
| chr10:155822
|
T | C | 75 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(72): Show | 75 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-20+20263T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155822 | ||||||
| chr10:155848
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-20+20289A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155848 | ||||||
| chr10:155946
|
T | TACTCCAT others(7): Show |
1 | a0001c0001t0001g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-20+20387_-20+2038 others(18): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 155946 | ||||||
| chr10:156014
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+20455C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156014 | ||||||
| chr10:156021
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0082 | 2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-20+20462A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156021 | ||||||
| chr10:156209
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG01123.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-20+20650A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156209 | ||||||
| chr10:156264
|
G | C | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+20705G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156264 | ||||||
| chr10:156268
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-20+20709C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156268 | ||||||
| chr10:156416
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(141): Show | 145 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-20+20857T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156416 | ||||||
| chr10:156550
|
T | G | 2 | a0001c0002t0001g0171a0001c0002t0001g0179 | 2 | NA18941.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-20+20991T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156550 | ||||||
| chr10:156603
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-20+21044A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156603 | ||||||
| chr10:156865
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.-20+21306A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156865 | ||||||
| chr10:156907
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+21348C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 156907 | ||||||
| chr10:157190
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20+21631G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157190 | ||||||
| chr10:157193
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+21634A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157193 | ||||||
| chr10:157230
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-20+21671C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157230 | ||||||
| chr10:157265
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-20+21706T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157265 | ||||||
| chr10:157426
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-20+21867C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157426 | ||||||
| chr10:157531
|
A | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-20+21972A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157531 | ||||||
| chr10:157676
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-20+22117C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157676 | ||||||
| chr10:157762
|
A | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+22203A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157762 | ||||||
| chr10:157860
|
T | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-22134T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 157860 | ||||||
| chr10:158241
|
G | C | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19-21753G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158241 | ||||||
| chr10:158412
|
C | CTT | 63 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-19-21564_-19-2156 others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158412 | |||||
| chr10:158418
|
T | A | 1 | a0001c0001t0001g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-19-21576T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158418 | ||||||
| chr10:158422
|
T | A | 4 | a0001c0001t0001g0314a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | NA18747.hp1 NA18972.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-21572T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158422 | ||||||
| chr10:158423
|
T | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-19-21571T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158423 | ||||||
| chr10:158470
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-21524G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158470 | ||||||
| chr10:158482
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19-21512G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158482 | ||||||
| chr10:158516
|
C | G | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19-21478C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158516 | ||||||
| chr10:158583
|
A | AT | 11 | a0001c0001t0001g0021a0001c0001t0001g0081a0001c0001t0001g0093others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-21393dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158583 | |||||
| chr10:158762
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-21232A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158762 | ||||||
| chr10:158964
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0100others(6): Show | 10 | HG01074.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-21030T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158964 | ||||||
| chr10:158984
|
G | GT | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(140): Show | 144 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-21004dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158984 | |||||
| chr10:158984
|
G | GTT | 46 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00673.hp2 HG00741.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.-19-21005_-19-2100 others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158984 | |||||
| chr10:158984
|
G | GTTT | 7 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0093others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-21006_-19-2100 others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158984 | |||||
| chr10:158984
|
G | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00544.hp1 HG00741.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-21010G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158984 | ||||||
| chr10:158989
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-19-21005T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158989 | ||||||
| chr10:158990
|
TG | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(56): Show | 60 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19-21003delG | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158990 | ||||||
| chr10:158991
|
G | GT | 6 | a0001c0002t0001g0149a0001c0002t0001g0159a0001c0002t0001g0238others(3): Show | 6 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-20986dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 158991 | |||||
| chr10:158991
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.-19-21003G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158991 | ||||||
| chr10:158995
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-19-20999T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 158995 | ||||||
| chr10:159130
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-19-20864C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159130 | ||||||
| chr10:159130
|
CT | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-20862delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 159130 | |||||
| chr10:159131
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-19-20863T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159131 | ||||||
| chr10:159133
|
A | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0112 | 2 | NA18974.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-19-20861A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159133 | ||||||
| chr10:159152
|
C | G | 1 | a0001c0001t0001g0331 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19-20842C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159152 | ||||||
| chr10:159361
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-19-20633C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159361 | ||||||
| chr10:159436
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-19-20558A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159436 | ||||||
| chr10:159913
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.-19-20081A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 159913 | ||||||
| chr10:160023
|
G | T | 1 | a0001c0001t0001g0104 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19-19971G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160023 | ||||||
| chr10:160146
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-19848A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160146 | ||||||
| chr10:160221
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-19773C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160221 | ||||||
| chr10:160245
|
G | C | 4 | a0001c0001t0001g0282a0001c0001t0001g0287a0001c0001t0001g0309others(1): Show | 4 | HG00642.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-19749G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160245 | ||||||
| chr10:160294
|
A | T | 2 | a0001c0001t0001g0282a0001c0001t0007g0283 | 2 | HG00642.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-19-19700A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160294 | ||||||
| chr10:160354
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-19-19640A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160354 | ||||||
| chr10:160429
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19-19565T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160429 | ||||||
| chr10:160613
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0102others(4): Show | 8 | HG01074.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-19381A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160613 | ||||||
| chr10:160638
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-19356G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160638 | ||||||
| chr10:160863
|
GC | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0097others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-19128delC | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160863 | |||||
| chr10:160917
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(222): Show | 226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.-19-19077C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160917 | ||||||
| chr10:160949
|
CT | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0339a0001c0002t0001g0154others(5): Show | 8 | HG01192.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-19015delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTT | C | 34 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0163others(31): Show | 35 | HG00597.hp1 HG00733.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19-19016_-19-1901 others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTT | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0183others(4): Show | 7 | HG00140.hp2 HG01891.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-19019_-19-1901 others(9): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTT | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(57): Show | 61 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-19-19020_-19-1901 others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0137others(6): Show | 9 | HG00558.hp2 HG00738.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-19023_-19-1901 others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTTT others(3): Show |
C | 76 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0083others(73): Show | 76 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-19-19024_-19-1901 others(14): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTTT others(4): Show |
C | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-19-19025_-19-1901 others(15): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0025a0001c0001t0001g0086a0001c0001t0001g0094 | 3 | HG01167.hp1 NA18951.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-19-19026_-19-1901 others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160949
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0053a0001c0001t0001g0059 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-19-19030_-19-1901 others(20): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 160949 | |||||
| chr10:160991
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19-19003G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 160991 | ||||||
| chr10:161038
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-19-18956T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161038 | ||||||
| chr10:161055
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0275 | 2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-19-18939C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161055 | ||||||
| chr10:161098
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-18896A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161098 | ||||||
| chr10:161105
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-19-18889G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161105 | ||||||
| chr10:161119
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-19-18875G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161119 | ||||||
| chr10:161326
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19-18668T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161326 | ||||||
| chr10:161377
|
G | A | 4 | a0001c0002t0001g0151a0001c0002t0001g0153a0001c0002t0001g0171others(1): Show | 4 | NA18941.hp2 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-18617G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161377 | ||||||
| chr10:161390
|
A | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-19-18604A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161390 | ||||||
| chr10:161503
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19-18491A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161503 | ||||||
| chr10:161513
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-18481A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161513 | ||||||
| chr10:161559
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0212others(4): Show | 8 | HG00738.hp1 HG01123.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-18435G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161559 | ||||||
| chr10:161642
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-19-18352C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161642 | ||||||
| chr10:161873
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-19-18121G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161873 | ||||||
| chr10:161889
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(39): Show | 43 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-18105T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161889 | ||||||
| chr10:161949
|
C | T | 18 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0153others(15): Show | 18 | HG00597.hp1 HG00733.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-18045C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 161949 | ||||||
| chr10:162260
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-17734C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162260 | ||||||
| chr10:162400
|
A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-17594A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162400 | ||||||
| chr10:162457
|
G | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0084others(15): Show | 19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-17537G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162457 | ||||||
| chr10:162470
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-17524C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162470 | ||||||
| chr10:162585
|
A | G | 1 | a0001c0002t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19-17409A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162585 | ||||||
| chr10:162774
|
T | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-17220T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162774 | ||||||
| chr10:162861
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-19-17133C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 162861 | ||||||
| chr10:163065
|
T | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0309 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-19-16929T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163065 | ||||||
| chr10:163508
|
C | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-19-16486C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163508 | ||||||
| chr10:163520
|
C | G | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19-16474C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163520 | ||||||
| chr10:163768
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-16226C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163768 | ||||||
| chr10:163784
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-19-16210A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163784 | ||||||
| chr10:163878
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-19-16116C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163878 | ||||||
| chr10:163952
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-16042C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 163952 | ||||||
| chr10:164263
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-19-15731C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164263 | ||||||
| chr10:164316
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19-15678G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164316 | ||||||
| chr10:164431
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-19-15563A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164431 | ||||||
| chr10:164439
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-19-15555T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164439 | ||||||
| chr10:164694
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-19-15300T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164694 | ||||||
| chr10:164702
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-15292G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164702 | ||||||
| chr10:164953
|
CAT | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-15040_-19-1503 others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 164953 | ||||||
| chr10:165014
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-19-14980G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165014 | ||||||
| chr10:165125
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19-14869T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165125 | ||||||
| chr10:165168
|
AAGAC | A | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-14823_-19-1482 others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 165168 | |||||
| chr10:165171
|
A | G | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 7 | NA18941.hp1 NA18945.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-14823A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165171 | ||||||
| chr10:165225
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-19-14769T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165225 | ||||||
| chr10:165268
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-19-14726C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165268 | ||||||
| chr10:165306
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-19-14688A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165306 | ||||||
| chr10:165323
|
TCCTAGTT others(8): Show |
T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-14665_-19-1465 others(19): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 165323 | |||||
| chr10:165525
|
C | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(2): Show | 5 | HG00558.hp2 NA18940.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-14469C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 165525 | ||||||
| chr10:166050
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-13944C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166050 | ||||||
| chr10:166095
|
A | G | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG01358.hp1 HG01496.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-13899A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166095 | ||||||
| chr10:166189
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-13805A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166189 | ||||||
| chr10:166190
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-13804A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166190 | ||||||
| chr10:166373
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19-13621T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166373 | ||||||
| chr10:166497
|
A | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-13497A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166497 | ||||||
| chr10:166652
|
A | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-13342A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166652 | ||||||
| chr10:166857
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19-13137A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 166857 | ||||||
| chr10:167034
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-19-12960G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167034 | ||||||
| chr10:167111
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0138 | 3 | HG02615.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-12883A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167111 | ||||||
| chr10:167112
|
A | G | 1 | a0001c0002t0001g0179 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-19-12882A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167112 | ||||||
| chr10:167212
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-12782T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167212 | ||||||
| chr10:167406
|
A | G | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-19-12588A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167406 | ||||||
| chr10:167466
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19-12528A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167466 | ||||||
| chr10:167482
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-19-12512A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167482 | ||||||
| chr10:167671
|
A | G | 1 | a0001c0002t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19-12323A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167671 | ||||||
| chr10:167782
|
T | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-12212T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167782 | ||||||
| chr10:167797
|
T | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-12197T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167797 | ||||||
| chr10:167808
|
T | G | 18 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0153others(15): Show | 18 | HG00597.hp1 HG00733.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-12186T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167808 | ||||||
| chr10:167838
|
T | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(331): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-19-12156T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167838 | ||||||
| chr10:167985
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-19-12009A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 167985 | ||||||
| chr10:168162
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0084others(14): Show | 18 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19-11832C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168162 | ||||||
| chr10:168415
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-11579C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168415 | ||||||
| chr10:168454
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-11540A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168454 | ||||||
| chr10:168781
|
A | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0034others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-19-11213A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168781 | ||||||
| chr10:168878
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-19-11116C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168878 | ||||||
| chr10:168926
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19-11068C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168926 | ||||||
| chr10:168960
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-11034T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 168960 | ||||||
| chr10:169104
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-10890A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169104 | ||||||
| chr10:169487
|
A | G | 1 | a0001c0002t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19-10507A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169487 | ||||||
| chr10:169568
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-19-10426G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169568 | ||||||
| chr10:169725
|
A | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0026others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19-10269A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169725 | ||||||
| chr10:169754
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-10240C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169754 | ||||||
| chr10:169765
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-19-10229A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169765 | ||||||
| chr10:169821
|
A | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-10173A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169821 | ||||||
| chr10:169952
|
CCAAG | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-19-10039_-19-1003 others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 169952 | |||||
| chr10:169961
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-19-10033C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 169961 | ||||||
| chr10:170233
|
A | C | 1 | a0001c0002t0001g0153 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-19-9761A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170233 | ||||||
| chr10:170243
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-9751T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170243 | ||||||
| chr10:170350
|
T | C | 8 | a0001c0001t0001g0263a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 8 | HG02040.hp2 HG02056.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-9644T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170350 | ||||||
| chr10:170380
|
CAG | C | 18 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0153others(15): Show | 18 | HG00597.hp1 HG00733.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-9612_-19-9611d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170380 | |||||
| chr10:170431
|
C | CGT | 301 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(298): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-19-9539_-19-9538d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170431 | |||||
| chr10:170431
|
C | CGTGT | 12 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0059others(9): Show | 12 | HG00280.hp2 HG01515.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19-9541_-19-9538d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170431 | |||||
| chr10:170431
|
C | CGTGTGT | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-9543_-19-9538d others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170431 | |||||
| chr10:170431
|
CGTGT | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-9541_-19-9538d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170431 | |||||
| chr10:170433
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-9561T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170433 | ||||||
| chr10:170464
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-9530A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170464 | ||||||
| chr10:170475
|
AAATG | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-19-9513_-19-9510d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 170475 | |||||
| chr10:170536
|
G | C | 11 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0198others(8): Show | 11 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-9458G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170536 | ||||||
| chr10:170619
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19-9375T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170619 | ||||||
| chr10:170740
|
A | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-9254A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170740 | ||||||
| chr10:170804
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-19-9190G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170804 | ||||||
| chr10:170957
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-9037A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 170957 | ||||||
| chr10:171092
|
G | A | 7 | a0001c0002t0001g0105a0001c0002t0001g0235a0001c0002t0001g0236others(4): Show | 7 | HG01074.hp2 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-8902G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171092 | ||||||
| chr10:171141
|
G | T | 34 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0264others(31): Show | 34 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.-19-8853G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171141 | ||||||
| chr10:171301
|
A | G | 77 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0263others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-19-8693A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171301 | ||||||
| chr10:171392
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-8602A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171392 | ||||||
| chr10:171468
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-8526A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171468 | ||||||
| chr10:171552
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-19-8442A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171552 | ||||||
| chr10:171783
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19-8211G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 171783 | ||||||
| chr10:172158
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-7836C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172158 | ||||||
| chr10:172183
|
G | C | 1 | a0001c0001t0001g0328 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-19-7811G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172183 | ||||||
| chr10:172225
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-19-7769G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172225 | ||||||
| chr10:172396
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-19-7598G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172396 | ||||||
| chr10:172437
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19-7557A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172437 | ||||||
| chr10:172496
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-19-7498A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172496 | ||||||
| chr10:172683
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-19-7311A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172683 | ||||||
| chr10:172685
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-19-7309G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172685 | ||||||
| chr10:172717
|
A | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-7277A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172717 | ||||||
| chr10:172852
|
T | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0245a0001c0001t0001g0261 | 3 | HG00544.hp2 NA18964.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-19-7142T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172852 | ||||||
| chr10:172916
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19-7078C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 172916 | ||||||
| chr10:173150
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19-6844A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173150 | ||||||
| chr10:173336
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-19-6658A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173336 | ||||||
| chr10:173392
|
T | G | 29 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0033others(26): Show | 29 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19-6602T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173392 | ||||||
| chr10:173496
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-19-6498A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173496 | ||||||
| chr10:173553
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-19-6441A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173553 | ||||||
| chr10:173570
|
A | C | 1 | a0001c0001t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-6424A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173570 | ||||||
| chr10:173618
|
G | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-6376G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173618 | ||||||
| chr10:173712
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-6282A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173712 | ||||||
| chr10:173723
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-6271A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173723 | ||||||
| chr10:173729
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-19-6265A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 173729 | ||||||
| chr10:174027
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5967C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174027 | ||||||
| chr10:174157
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5837C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174157 | ||||||
| chr10:174195
|
C | A | 2 | a0001c0001t0001g0282a0001c0001t0007g0283 | 2 | HG00642.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-19-5799C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174195 | ||||||
| chr10:174471
|
A | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-19-5523A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174471 | ||||||
| chr10:174497
|
A | C | 2 | a0001c0002t0001g0159a0001c0002t0001g0178 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-5497A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174497 | ||||||
| chr10:174509
|
CACTACAG others(93): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19-5421_-19-5322d others(102): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 174509 | |||||
| chr10:174702
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5292C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174702 | ||||||
| chr10:174705
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5289T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174705 | ||||||
| chr10:174707
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5287A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174707 | ||||||
| chr10:174709
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5285T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174709 | ||||||
| chr10:174723
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5271A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174723 | ||||||
| chr10:174805
|
CGGGCACT others(43): Show |
C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-5054_-19-5005d others(52): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 174805 | |||||
| chr10:174811
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-19-5183C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174811 | ||||||
| chr10:174939
|
C | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | NA18989.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-19-5055C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174939 | ||||||
| chr10:174940
|
A | ATTGGTCA others(43): Show |
66 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(63): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-4986_-19-4937d others(52): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 174940 | |||||
| chr10:174940
|
A | G | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-5054A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 174940 | ||||||
| chr10:175037
|
T | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0138 | 3 | HG02615.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-4957T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175037 | ||||||
| chr10:175225
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-19-4769G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175225 | ||||||
| chr10:175328
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19-4666G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175328 | ||||||
| chr10:175395
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-4599C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175395 | ||||||
| chr10:175460
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-4534A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175460 | ||||||
| chr10:175534
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0026others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-19-4460A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175534 | ||||||
| chr10:175938
|
A | C | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-4056A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175938 | ||||||
| chr10:175953
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19-4041C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 175953 | ||||||
| chr10:176065
|
T | A | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19-3929T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176065 | ||||||
| chr10:176071
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0066 | 3 | NA18942.hp2 NA18955.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-19-3923T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176071 | ||||||
| chr10:176389
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-3605T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176389 | ||||||
| chr10:176630
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | NA18989.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-19-3364A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176630 | ||||||
| chr10:176804
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-3190T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176804 | ||||||
| chr10:176885
|
G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0335 | 3 | HG03927.hp1 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-19-3109G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176885 | ||||||
| chr10:176981
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-19-3013T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 176981 | ||||||
| chr10:177218
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-2776C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 177218 | ||||||
| chr10:177424
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19-2570G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 177424 | ||||||
| chr10:177849
|
C | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-19-2145C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 177849 | ||||||
| chr10:177937
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19-2057T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 177937 | ||||||
| chr10:178056
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02886.hp1 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-19-1938C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178056 | ||||||
| chr10:178115
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19-1879C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178115 | ||||||
| chr10:178276
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0109 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1718A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178276 | ||||||
| chr10:178299
|
C | T | 74 | a0001c0001t0001g0188a0001c0001t0001g0264a0001c0001t0001g0265others(71): Show | 74 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-19-1695C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178299 | ||||||
| chr10:178315
|
C | T | 61 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(58): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-19-1679C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178315 | ||||||
| chr10:178557
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19-1437T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178557 | ||||||
| chr10:178619
|
C | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01358.hp1 HG01496.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1375C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178619 | ||||||
| chr10:178771
|
A | G | 1 | a0001c0002t0001g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-19-1223A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178771 | ||||||
| chr10:178909
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-1085G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178909 | ||||||
| chr10:178912
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19-1082G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 178912 | ||||||
| chr10:179021
|
A | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0081others(2): Show | 5 | NA18954.hp1 NA18967.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-973A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 179021 | ||||||
| chr10:179050
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-944T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 179050 | ||||||
| chr10:179168
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-19-826A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 179168 | ||||||
| chr10:179586
|
ATAAAC | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0087others(13): Show | 16 | HG00544.hp1 HG02071.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-403_-19-399del others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 179586 | |||||
| chr10:179719
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-19-275G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 179719 | ||||||
| chr10:179771
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-19-223A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 1/14 | chr10 | 179771 | ||||||
| chr10:180148
|
A | G | 3 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0334 | 3 | HG02080.hp2 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.116+20A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180148 | ||||||
| chr10:180218
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+90C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180218 | ||||||
| chr10:180284
|
C | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.116+156C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180284 | ||||||
| chr10:180430
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0128 | 2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.116+302C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180430 | ||||||
| chr10:180455
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116+327G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180455 | ||||||
| chr10:180473
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+345C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180473 | ||||||
| chr10:180557
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.116+429G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180557 | ||||||
| chr10:180617
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.116+489T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180617 | ||||||
| chr10:180645
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+517C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180645 | ||||||
| chr10:180711
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.116+583T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 180711 | ||||||
| chr10:181008
|
A | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.116+880A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 181008 | ||||||
| chr10:181147
|
T | A | 11 | a0001c0001t0001g0026a0001c0001t0001g0087a0001c0001t0001g0088others(8): Show | 11 | NA18968.hp1 NA18970.hp1 NA18974.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+1019T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 181147 | ||||||
| chr10:181192
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.116+1064G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 181192 | ||||||
| chr10:181372
|
A | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(38): Show | 42 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.116+1244A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 181372 | ||||||
| chr10:181771
|
G | GA | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1651dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 181771 | |||||
| chr10:181905
|
T | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.116+1777T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 181905 | ||||||
| chr10:182249
|
A | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.116+2121A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182249 | ||||||
| chr10:182276
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116+2148A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182276 | ||||||
| chr10:182506
|
TGAAAAA | T | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.116+2389_116+2394d others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 182506 | |||||
| chr10:182564
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0147 | 3 | NA19056.hp2 NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.116+2436C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182564 | ||||||
| chr10:182685
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.116+2557G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182685 | ||||||
| chr10:182715
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116+2587C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182715 | ||||||
| chr10:182844
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+2716C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 182844 | ||||||
| chr10:183071
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+2943C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 183071 | ||||||
| chr10:183224
|
G | GT | 6 | a0001c0001t0001g0005a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+3111dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 183224 | |||||
| chr10:183246
|
G | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0087a0001c0001t0001g0088others(8): Show | 11 | NA18968.hp1 NA18970.hp1 NA18974.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+3118G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 183246 | ||||||
| chr10:183645
|
A | G | 7 | a0001c0002t0001g0105a0001c0002t0001g0235a0001c0002t0001g0236others(4): Show | 7 | HG01074.hp2 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+3517A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 183645 | ||||||
| chr10:183732
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+3604A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 183732 | ||||||
| chr10:183741
|
C | T | 73 | a0001c0001t0001g0188a0001c0001t0001g0264a0001c0001t0001g0265others(70): Show | 73 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.116+3613C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 183741 | ||||||
| chr10:184143
|
A | T | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+4015A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 184143 | ||||||
| chr10:184605
|
G | C | 1 | a0001c0001t0004g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.116+4477G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 184605 | ||||||
| chr10:184685
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0043others(3): Show | 6 | HG01192.hp2 HG01433.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4557T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 184685 | ||||||
| chr10:184899
|
G | GT | 100 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.116+4780dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 184899 | |||||
| chr10:185156
|
T | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0258 | 2 | HG01346.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.116+5028T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185156 | ||||||
| chr10:185336
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01358.hp1 HG01496.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+5208C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185336 | ||||||
| chr10:185388
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.116+5260T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185388 | ||||||
| chr10:185453
|
C | T | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+5325C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185453 | ||||||
| chr10:185493
|
T | TA | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0111others(12): Show | 15 | HG01891.hp2 HG01952.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+5381dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185493 | |||||
| chr10:185493
|
T | TAA | 63 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.116+5380_116+5381d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185493 | |||||
| chr10:185530
|
C | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(61): Show | 65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.116+5402C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185530 | ||||||
| chr10:185538
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.116+5410G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185538 | ||||||
| chr10:185611
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+5483C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185611 | ||||||
| chr10:185771
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+5643C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185771 | ||||||
| chr10:185813
|
C | CA | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.116+5692dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185813 | |||||
| chr10:185813
|
C | CAA | 81 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0038others(78): Show | 81 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.116+5691_116+5692d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185813 | |||||
| chr10:185813
|
C | CAAA | 5 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0001g0329others(2): Show | 5 | HG02055.hp2 HG02080.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+5690_116+5692d others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185813 | |||||
| chr10:185821
|
C | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.116+5693C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185821 | ||||||
| chr10:185827
|
A | AAAC | 4 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(1): Show | 4 | NA18940.hp2 NA18977.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+5700_116+5701i others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 185827 | |||||
| chr10:185868
|
C | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.116+5740C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185868 | ||||||
| chr10:185954
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0309 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.116+5826A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 185954 | ||||||
| chr10:186007
|
C | CT | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0265others(3): Show | 6 | HG00735.hp1 HG01257.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5894dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186007 | |||||
| chr10:186017
|
T | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.116+5889T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186017 | ||||||
| chr10:186065
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(2): Show | 5 | HG00558.hp2 NA18940.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+5937A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186065 | ||||||
| chr10:186301
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.116+6173G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186301 | ||||||
| chr10:186302
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG01123.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.116+6174C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186302 | ||||||
| chr10:186327
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.116+6199C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186327 | ||||||
| chr10:186556
|
A | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.116+6428A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186556 | ||||||
| chr10:186573
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.116+6445G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186573 | ||||||
| chr10:186632
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6504A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186632 | ||||||
| chr10:186642
|
C | CA | 13 | a0001c0001t0001g0157a0001c0002t0001g0147a0001c0002t0001g0148others(10): Show | 13 | HG00597.hp1 HG00733.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.116+6551dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAA | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0001g0185others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.116+6546_116+6551d others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(46): Show | 50 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.116+6545_116+6551d others(9): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+6541_116+6551d others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0163a0001c0001t0001g0170a0001c0001t0001g0173others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+6538_116+6551d others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116+6537_116+6551d others(17): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.116+6535_116+6551d others(19): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(11): Show |
C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+6534_116+6551d others(20): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(12): Show |
C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(186): Show | 190 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.116+6533_116+6551d others(21): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186642
|
CAAAAAAA others(13): Show |
C | 27 | a0001c0001t0001g0036a0001c0001t0001g0270a0001c0001t0001g0281others(24): Show | 27 | HG00673.hp2 HG00735.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.116+6532_116+6551d others(22): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 186642 | |||||
| chr10:186676
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6548A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186676 | ||||||
| chr10:186750
|
C | T | 7 | a0001c0001t0001g0181a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | NA18940.hp1 NA18953.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+6622C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186750 | ||||||
| chr10:186995
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.116+6867A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 186995 | ||||||
| chr10:187007
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.116+6879C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187007 | ||||||
| chr10:187059
|
C | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.116+6931C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187059 | ||||||
| chr10:187217
|
A | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.116+7089A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187217 | ||||||
| chr10:187260
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+7132A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187260 | ||||||
| chr10:187268
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.116+7140T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187268 | ||||||
| chr10:187361
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116+7233G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187361 | ||||||
| chr10:187362
|
C | T | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0323others(3): Show | 6 | HG02040.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+7234C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187362 | ||||||
| chr10:187430
|
C | G | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.116+7302C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187430 | ||||||
| chr10:187440
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0078 | 2 | HG00280.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.116+7312T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187440 | ||||||
| chr10:187497
|
G | A | 2 | a0001c0002t0001g0159a0001c0002t0001g0178 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.116+7369G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187497 | ||||||
| chr10:187600
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0076 | 2 | NA18953.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.116+7472A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187600 | ||||||
| chr10:187603
|
C | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.116+7475C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187603 | ||||||
| chr10:187604
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0076 | 2 | NA18953.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.116+7476G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187604 | ||||||
| chr10:187633
|
CA | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0110others(12): Show | 15 | HG00544.hp2 HG00738.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+7521delA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 187633 | |||||
| chr10:187633
|
CAA | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.116+7520_116+7521d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 187633 | |||||
| chr10:187833
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.116+7705G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187833 | ||||||
| chr10:187987
|
G | A | 1 | a0001c0002t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.116+7859G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 187987 | ||||||
| chr10:188301
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.116+8173A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188301 | ||||||
| chr10:188339
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.116+8211C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188339 | ||||||
| chr10:188424
|
CA | C | 18 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0153others(15): Show | 18 | HG00597.hp1 HG00733.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.116+8307delA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 188424 | |||||
| chr10:188435
|
A | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0122a0001c0001t0001g0278 | 3 | HG01243.hp2 HG03492.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.116+8307A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188435 | ||||||
| chr10:188449
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.116+8321C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188449 | ||||||
| chr10:188514
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116+8386G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188514 | ||||||
| chr10:188591
|
CA | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.116+8482delA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 188591 | |||||
| chr10:188610
|
AT | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(52): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.116+8485delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 188610 | |||||
| chr10:188611
|
T | A | 12 | a0001c0001t0001g0108a0001c0001t0001g0180a0001c0001t0001g0181others(9): Show | 12 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.116+8483T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188611 | ||||||
| chr10:188651
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+8523C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188651 | ||||||
| chr10:188690
|
T | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0080 | 3 | HG00597.hp2 HG02523.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.116+8562T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188690 | ||||||
| chr10:188876
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116+8748T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 188876 | ||||||
| chr10:189137
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0268 | 2 | HG01169.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.116+9009C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189137 | ||||||
| chr10:189204
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.116+9076T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189204 | ||||||
| chr10:189258
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.116+9130A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189258 | ||||||
| chr10:189334
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.116+9206C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189334 | ||||||
| chr10:189387
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0078 | 2 | HG00280.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.116+9259G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189387 | ||||||
| chr10:189435
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18952.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.116+9307A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189435 | ||||||
| chr10:189473
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.116+9345G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189473 | ||||||
| chr10:189520
|
ATTGT | A | 3 | a0001c0002t0001g0165a0001c0002t0001g0237a0001c0003t0001g0167 | 3 | HG00597.hp1 NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.116+9395_116+9398d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 189520 | |||||
| chr10:189646
|
A | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.116+9518A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189646 | ||||||
| chr10:189961
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.116+9833T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 189961 | ||||||
| chr10:189975
|
A | AG | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0057others(2): Show | 5 | HG00609.hp1 NA18949.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+9850dupG | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 189975 | |||||
| chr10:190157
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116+10029G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190157 | ||||||
| chr10:190200
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020 | 3 | HG01109.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+10072T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190200 | ||||||
| chr10:190368
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.116+10240C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190368 | ||||||
| chr10:190373
|
T | C | 1 | a0001c0002t0001g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.116+10245T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190373 | ||||||
| chr10:190512
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(38): Show | 42 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.116+10384C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190512 | ||||||
| chr10:190671
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.116+10543G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190671 | ||||||
| chr10:190693
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020 | 3 | HG01109.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+10565G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190693 | ||||||
| chr10:190976
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.116+10848G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 190976 | ||||||
| chr10:191445
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.116+11317C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191445 | ||||||
| chr10:191452
|
A | T | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.116+11324A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191452 | ||||||
| chr10:191642
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116+11514G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191642 | ||||||
| chr10:191707
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(2): Show | 5 | HG00558.hp2 NA18940.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+11579A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191707 | ||||||
| chr10:191810
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.116+11682G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191810 | ||||||
| chr10:191904
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020 | 3 | HG01109.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+11776G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 191904 | ||||||
| chr10:192178
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020 | 3 | HG01109.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.116+12050C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 192178 | ||||||
| chr10:192236
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116+12108G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 192236 | ||||||
| chr10:192319
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+12191T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 192319 | ||||||
| chr10:192414
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.116+12286T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 192414 | ||||||
| chr10:192901
|
A | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.116+12773A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 192901 | ||||||
| chr10:193026
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116+12898A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 193026 | ||||||
| chr10:193196
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.116+13068G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 193196 | ||||||
| chr10:193365
|
T | C | 1 | a0001c0002t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.116+13237T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 193365 | ||||||
| chr10:193505
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+13377G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 193505 | ||||||
| chr10:194406
|
G | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.116+14278G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 194406 | ||||||
| chr10:194543
|
A | G | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0335 | 3 | HG03927.hp1 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.116+14415A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 194543 | ||||||
| chr10:194735
|
A | AT | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+14614dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 194735 | |||||
| chr10:194848
|
T | G | 80 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(77): Show | 80 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.116+14720T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 194848 | ||||||
| chr10:195039
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.117-14850C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 195039 | ||||||
| chr10:195320
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0075others(3): Show | 6 | NA18962.hp2 NA18972.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-14569C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 195320 | ||||||
| chr10:195562
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.117-14327A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 195562 | ||||||
| chr10:195759
|
T | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0335 | 3 | HG03927.hp1 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.117-14130T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 195759 | ||||||
| chr10:196273
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0284a0001c0001t0001g0285others(1): Show | 4 | HG02630.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-13616C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196273 | ||||||
| chr10:196315
|
A | G | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117-13574A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196315 | ||||||
| chr10:196379
|
A | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-13510A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196379 | ||||||
| chr10:196461
|
A | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0047others(16): Show | 19 | HG02071.hp1 HG02080.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.117-13428A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196461 | ||||||
| chr10:196529
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-13360A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196529 | ||||||
| chr10:196704
|
T | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG01358.hp1 HG01496.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-13185T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196704 | ||||||
| chr10:196801
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-13088C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196801 | ||||||
| chr10:196890
|
C | A | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-12999C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196890 | ||||||
| chr10:196898
|
C | A | 94 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.117-12991C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196898 | ||||||
| chr10:196919
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.117-12970C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196919 | ||||||
| chr10:196979
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0121 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.117-12910A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196979 | ||||||
| chr10:196984
|
A | ATTCATGT others(149): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0286 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117-12867_117-1286 others(160): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 196984 | |||||
| chr10:196998
|
A | C | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.117-12891A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 196998 | ||||||
| chr10:197049
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-12840A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197049 | ||||||
| chr10:197058
|
ATGTGTTC others(149): Show |
A | 2 | a0001c0002t0001g0159a0001c0002t0001g0178 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.117-12788_117-1263 others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197058 | |||||
| chr10:197062
|
GTTCATGT others(71): Show |
G | 4 | a0001c0002t0001g0151a0001c0002t0001g0153a0001c0002t0001g0171others(1): Show | 4 | NA18941.hp2 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-12799_117-1272 others(82): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197062 | |||||
| chr10:197154
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117-12735A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197154 | ||||||
| chr10:197168
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.117-12721G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197168 | ||||||
| chr10:197178
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0101a0001c0001t0001g0136 | 3 | HG02809.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.117-12711G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197178 | ||||||
| chr10:197194
|
C | CGTGTGTG others(305): Show |
77 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 77 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.117-12618_117-1261 others(316): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197194 | |||||
| chr10:197194
|
C | CGTGTGTG others(617): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0059 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.117-12618_117-1261 others(628): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197194 | |||||
| chr10:197194
|
C | CGTGTGTG others(305): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0128 | 2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.117-12618_117-1261 others(316): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197194 | |||||
| chr10:197194
|
C | CGTGTGTG others(305): Show |
1 | a0001c0001t0001g0133 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.117-12644_117-1264 others(316): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 197194 | |||||
| chr10:197194
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 210 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.117-12695C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197194 | ||||||
| chr10:197272
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.117-12617T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197272 | ||||||
| chr10:197463
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.117-12426A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197463 | ||||||
| chr10:197509
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117-12380C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197509 | ||||||
| chr10:197877
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117-12012T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 197877 | ||||||
| chr10:198040
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0134 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.117-11849G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198040 | ||||||
| chr10:198090
|
T | A | 1 | a0001c0001t0001g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.117-11799T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198090 | ||||||
| chr10:198388
|
A | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.117-11501A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198388 | ||||||
| chr10:198389
|
A | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-11500A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198389 | ||||||
| chr10:198594
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117-11295A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198594 | ||||||
| chr10:198621
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(217): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.117-11268A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198621 | ||||||
| chr10:198801
|
A | G | 1 | a0001c0001t0005g0304 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.117-11088A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198801 | ||||||
| chr10:198944
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117-10945C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198944 | ||||||
| chr10:198986
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.117-10903C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198986 | ||||||
| chr10:198990
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117-10899T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 198990 | ||||||
| chr10:199103
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.117-10786C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199103 | ||||||
| chr10:199154
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-10735T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199154 | ||||||
| chr10:199244
|
C | T | 3 | a0001c0002t0001g0238a0001c0002t0001g0239a0001c0002t0001g0240 | 3 | HG01192.hp1 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117-10645C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199244 | ||||||
| chr10:199258
|
T | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0128 | 2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.117-10631T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199258 | ||||||
| chr10:199309
|
TCCTC | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.117-10563_117-1056 others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 199309 | |||||
| chr10:199309
|
TCCTCCCT others(17): Show |
T | 1 | a0001c0001t0001g0195 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.117-10574_117-1055 others(28): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 199309 | |||||
| chr10:199313
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117-10576C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199313 | ||||||
| chr10:199327
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.117-10562C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199327 | ||||||
| chr10:199330
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117-10559T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199330 | ||||||
| chr10:199338
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.117-10551C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199338 | ||||||
| chr10:199603
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.117-10286A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199603 | ||||||
| chr10:199702
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117-10187G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 199702 | ||||||
| chr10:199830
|
CT | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.117-10052delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 199830 | |||||
| chr10:199872
|
TTCTTTTT others(12): Show |
T | 78 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.117-10012_117-9994 others(22): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 199872 | |||||
| chr10:200205
|
G | GGGGTGTG others(9): Show |
1 | a0001c0001t0002g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.117-9683_117-9682i others(18): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGGGTGTG others(11): Show |
1 | a0001c0001t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.117-9683_117-9682i others(20): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGGGTGTG others(27): Show |
1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117-9683_117-9682i others(36): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(1): Show |
37 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0026others(34): Show | 37 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.117-9671_117-9664d others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(3): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0102others(1): Show | 5 | HG02109.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-9673_117-9664d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.117-9677_117-9664d others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(9): Show |
76 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.117-9679_117-9664d others(18): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(11): Show |
68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.117-9681_117-9664d others(20): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(13): Show |
30 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0042others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.117-9683_117-9664d others(22): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(15): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-9664_117-9663i others(24): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(17): Show |
6 | a0001c0001t0001g0192a0001c0001t0001g0198a0001c0001t0001g0203others(3): Show | 6 | HG00544.hp2 NA18949.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-9664_117-9663i others(26): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(19): Show |
44 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0108others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.117-9664_117-9663i others(28): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(21): Show |
9 | a0001c0001t0001g0194a0001c0001t0001g0206a0001c0001t0001g0215others(6): Show | 10 | HG00438.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-9664_117-9663i others(30): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(23): Show |
1 | a0001c0001t0001g0217 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.117-9664_117-9663i others(32): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GGTGTGTG others(25): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0243 | 3 | HG00738.hp1 HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.117-9664_117-9663i others(34): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200205
|
G | GTGTGTGT others(20): Show |
1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.117-9684_117-9683i others(29): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200205 | ||||||
| chr10:200205
|
GGTGT | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-9667_117-9664d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200205 | |||||
| chr10:200287
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.117-9602G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200287 | ||||||
| chr10:200318
|
C | CAT | 326 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(323): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.117-9567_117-9566d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200318 | |||||
| chr10:200318
|
C | CATATATA others(20): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0102others(1): Show | 5 | HG02109.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-9566_117-9565i others(29): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 200318 | |||||
| chr10:200382
|
A | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0204a0001c0001t0001g0214 | 3 | NA18947.hp1 NA18949.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.117-9507A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200382 | ||||||
| chr10:200431
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-9458A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200431 | ||||||
| chr10:200572
|
C | T | 36 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(33): Show | 37 | HG00597.hp1 HG00733.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.117-9317C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200572 | ||||||
| chr10:200619
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.117-9270A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200619 | ||||||
| chr10:200993
|
G | A | 75 | a0001c0001t0001g0188a0001c0001t0001g0264a0001c0001t0001g0265others(72): Show | 75 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.117-8896G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 200993 | ||||||
| chr10:201306
|
G | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-8583G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201306 | ||||||
| chr10:201374
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0212 | 3 | HG01346.hp2 HG01993.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-8515C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201374 | ||||||
| chr10:201537
|
T | C | 4 | a0001c0001t0001g0313a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02040.hp2 HG02071.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-8352T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201537 | ||||||
| chr10:201585
|
T | TAC | 12 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0047others(9): Show | 12 | HG01255.hp1 HG02080.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.117-8284_117-8283d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(1): Show |
63 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0106others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.117-8290_117-8283d others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(3): Show |
56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0137others(53): Show | 56 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.117-8292_117-8283d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(5): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG00741.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-8294_117-8283d others(14): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(9): Show |
9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0066others(6): Show | 9 | HG01891.hp1 HG02647.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.117-8298_117-8283d others(18): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(11): Show |
20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(17): Show | 21 | HG00323.hp2 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.117-8300_117-8283d others(20): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(13): Show |
21 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0026others(18): Show | 21 | HG00140.hp1 HG00544.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.117-8302_117-8283d others(22): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(15): Show |
55 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0020others(52): Show | 55 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.117-8283_117-8282i others(24): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(17): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(12): Show | 15 | HG01192.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-8283_117-8282i others(26): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(19): Show |
1 | a0001c0001t0001g0078 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117-8283_117-8282i others(28): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(21): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0057 | 2 | HG01496.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.117-8283_117-8282i others(30): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201585
|
T | TACACACA others(23): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0125 | 3 | HG00609.hp1 NA18949.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.117-8283_117-8282i others(32): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 201585 | |||||
| chr10:201606
|
A | ACACACAC others(7): Show |
7 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0270others(4): Show | 7 | HG01257.hp1 HG01517.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-8283_117-8282i others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201606 | ||||||
| chr10:201606
|
A | ACACACAC others(5): Show |
24 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0313others(21): Show | 24 | HG00673.hp2 HG02040.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.117-8283_117-8282i others(14): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201606 | ||||||
| chr10:201607
|
T | A | 31 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0265others(28): Show | 31 | HG00673.hp2 HG01257.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.117-8282T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201607 | ||||||
| chr10:201607
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117-8282T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201607 | ||||||
| chr10:201716
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.117-8173G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 201716 | ||||||
| chr10:202345
|
T | C | 20 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG00639.hp2 HG01257.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.117-7544T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202345 | ||||||
| chr10:202389
|
A | C | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0288others(8): Show | 11 | HG02257.hp1 HG02647.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-7500A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202389 | ||||||
| chr10:202541
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117-7348A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202541 | ||||||
| chr10:202566
|
G | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.117-7323G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202566 | ||||||
| chr10:202747
|
A | G | 20 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0067others(17): Show | 20 | HG00544.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.117-7142A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202747 | ||||||
| chr10:202858
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117-7031T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202858 | ||||||
| chr10:202878
|
T | G | 1 | a0001c0002t0001g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.117-7011T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202878 | ||||||
| chr10:202889
|
T | G | 1 | a0001c0001t0007g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117-7000T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 202889 | ||||||
| chr10:202971
|
T | TA | 9 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.117-6909dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 202971 | |||||
| chr10:203187
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.117-6702C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203187 | ||||||
| chr10:203228
|
G | A | 336 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.117-6661G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203228 | ||||||
| chr10:203632
|
A | C | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117-6257A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203632 | ||||||
| chr10:203632
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(217): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.117-6257A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203632 | ||||||
| chr10:203736
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.117-6153C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203736 | ||||||
| chr10:203844
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.117-6045T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 203844 | ||||||
| chr10:204153
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.117-5736T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204153 | ||||||
| chr10:204207
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.117-5682G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204207 | ||||||
| chr10:204219
|
T | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0245a0001c0001t0001g0261 | 3 | HG00544.hp2 NA18964.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.117-5670T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204219 | ||||||
| chr10:204264
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0134 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.117-5625T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204264 | ||||||
| chr10:204929
|
A | T | 1 | a0001c0001t0001g0005 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.117-4960A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204929 | ||||||
| chr10:204981
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.117-4908G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 204981 | ||||||
| chr10:205064
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.117-4825G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205064 | ||||||
| chr10:205093
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117-4796C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205093 | ||||||
| chr10:205400
|
A | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-4489A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205400 | ||||||
| chr10:205481
|
A | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-4408A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205481 | ||||||
| chr10:205638
|
C | T | 36 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(33): Show | 37 | HG00597.hp1 HG00733.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.117-4251C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205638 | ||||||
| chr10:205750
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0286 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117-4139A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205750 | ||||||
| chr10:205794
|
CT | C | 8 | a0001c0001t0001g0138a0001c0002t0001g0105a0001c0002t0001g0235others(5): Show | 8 | HG01074.hp2 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-4084delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 205794 | |||||
| chr10:205869
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117-4020T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 205869 | ||||||
| chr10:206014
|
G | GT | 15 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 16 | HG00558.hp2 HG00597.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.117-3859dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 206014 | |||||
| chr10:206017
|
T | G | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-3872T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206017 | ||||||
| chr10:206026
|
T | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.117-3863T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206026 | ||||||
| chr10:206027
|
T | G | 3 | a0001c0001t0001g0295a0001c0001t0002g0144a0001c0001t0002g0145 | 3 | HG00735.hp1 HG02723.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.117-3862T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206027 | ||||||
| chr10:206110
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.117-3779G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206110 | ||||||
| chr10:206221
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0008g0069 | 3 | NA18967.hp2 NA19062.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.117-3668G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206221 | ||||||
| chr10:206257
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-3632G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206257 | ||||||
| chr10:206277
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117-3612T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206277 | ||||||
| chr10:206326
|
C | T | 1 | a0001c0002t0001g0147 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.117-3563C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206326 | ||||||
| chr10:206496
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.117-3393T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206496 | ||||||
| chr10:206590
|
A | G | 4 | a0001c0001t0001g0330a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG00673.hp2 NA18945.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-3299A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206590 | ||||||
| chr10:206592
|
C | A | 1 | a0001c0002t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.117-3297C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206592 | ||||||
| chr10:206694
|
TTTGTATT others(3): Show |
T | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117-3193_117-3184d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 206694 | |||||
| chr10:206742
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-3147C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206742 | ||||||
| chr10:206749
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117-3140C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206749 | ||||||
| chr10:206753
|
T | C | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-3136T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206753 | ||||||
| chr10:206973
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.117-2916T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 206973 | ||||||
| chr10:207283
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.117-2606G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207283 | ||||||
| chr10:207427
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-2462A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207427 | ||||||
| chr10:207474
|
G | A | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-2415G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207474 | ||||||
| chr10:207591
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.117-2298A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207591 | ||||||
| chr10:207608
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-2281C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207608 | ||||||
| chr10:207679
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.117-2210C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207679 | ||||||
| chr10:207750
|
C | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-2139C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207750 | ||||||
| chr10:207780
|
G | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0067others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.117-2109G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207780 | ||||||
| chr10:207831
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117-2058A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207831 | ||||||
| chr10:207900
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.117-1989C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207900 | ||||||
| chr10:207948
|
C | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.117-1941C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207948 | ||||||
| chr10:207959
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG01123.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.117-1930A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 207959 | ||||||
| chr10:208477
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.117-1412A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 208477 | ||||||
| chr10:208484
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117-1405A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 208484 | ||||||
| chr10:208977
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.117-912A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 208977 | ||||||
| chr10:209003
|
A | ATG | 7 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 8 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-870_117-869dup others(2): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 209003 | |||||
| chr10:209021
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.117-868A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209021 | ||||||
| chr10:209048
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117-841T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209048 | ||||||
| chr10:209050
|
T | G | 52 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0031others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.117-839T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209050 | ||||||
| chr10:209052
|
G | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0082others(8): Show | 11 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.117-837G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209052 | ||||||
| chr10:209066
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.117-823T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209066 | ||||||
| chr10:209282
|
T | C | 81 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(78): Show | 81 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.117-607T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209282 | ||||||
| chr10:209309
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-580G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209309 | ||||||
| chr10:209379
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.117-510A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209379 | ||||||
| chr10:209492
|
A | G | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-397A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209492 | ||||||
| chr10:209746
|
G | A | 13 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(10): Show | 13 | HG01074.hp2 HG01192.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.117-143G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209746 | ||||||
| chr10:209747
|
TTCTTTA | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.117-137_117-132del others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 209747 | |||||
| chr10:209748
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.117-141T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209748 | ||||||
| chr10:209759
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.117-130T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 2/14 | chr10 | 209759 | ||||||
| chr10:210141
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.276+93T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210141 | ||||||
| chr10:210179
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+131C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210179 | ||||||
| chr10:210257
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.276+209A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210257 | ||||||
| chr10:210674
|
G | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.276+626G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210674 | ||||||
| chr10:210722
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0118 | 2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.276+674G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210722 | ||||||
| chr10:210744
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.276+696A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210744 | ||||||
| chr10:210957
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.276+909G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 210957 | ||||||
| chr10:211008
|
A | C | 2 | a0001c0002t0001g0171a0001c0002t0001g0179 | 2 | NA18941.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.276+960A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 211008 | ||||||
| chr10:211018
|
C | T | 80 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(77): Show | 80 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.276+970C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 211018 | ||||||
| chr10:211096
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.276+1048G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 211096 | ||||||
| chr10:211225
|
A | T | 1 | a0001c0001t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.276+1177A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 211225 | ||||||
| chr10:211406
|
ATCTTATA others(6): Show |
A | 1 | a0001c0002t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.276+1363_276+1375d others(15): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 211406 | |||||
| chr10:211564
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.276+1516C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 211564 | ||||||
| chr10:212433
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0268 | 2 | HG01169.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.276+2385T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 212433 | ||||||
| chr10:212578
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.276+2530C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 212578 | ||||||
| chr10:212707
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276+2659A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 212707 | ||||||
| chr10:212875
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.276+2827C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 212875 | ||||||
| chr10:213127
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276+3079C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 213127 | ||||||
| chr10:213847
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.276+3799T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 213847 | ||||||
| chr10:213961
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.276+3913G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 213961 | ||||||
| chr10:214104
|
T | C | 37 | a0001c0001t0001g0081a0001c0001t0001g0184a0001c0001t0001g0188others(34): Show | 37 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.276+4056T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214104 | ||||||
| chr10:214321
|
A | T | 1 | a0001c0001t0001g0263 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.276+4273A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214321 | ||||||
| chr10:214587
|
T | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.276+4539T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214587 | ||||||
| chr10:214597
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.276+4549A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214597 | ||||||
| chr10:214604
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(216): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.276+4556G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214604 | ||||||
| chr10:214648
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.276+4600C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214648 | ||||||
| chr10:214672
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.276+4624T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214672 | ||||||
| chr10:214824
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.276+4776G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214824 | ||||||
| chr10:214825
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.276+4777T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214825 | ||||||
| chr10:214901
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.276+4853T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 214901 | ||||||
| chr10:215048
|
G | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+5000G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215048 | ||||||
| chr10:215184
|
CTTAAAAT others(116): Show |
C | 1 | a0001c0001t0001g0033 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.276+5157_276+5279d others(2): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 215184 | |||||
| chr10:215205
|
C | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(38): Show | 42 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.276+5157C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215205 | ||||||
| chr10:215413
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276+5365C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215413 | ||||||
| chr10:215458
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.276+5410A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215458 | ||||||
| chr10:215475
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.276+5427A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215475 | ||||||
| chr10:215561
|
G | GT | 6 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0068others(3): Show | 6 | HG00597.hp2 HG02602.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+5527dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 215561 | |||||
| chr10:215710
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.277-5485A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215710 | ||||||
| chr10:215855
|
C | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.277-5340C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 215855 | ||||||
| chr10:216080
|
T | G | 2 | a0001c0002t0001g0159a0001c0002t0001g0178 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.277-5115T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216080 | ||||||
| chr10:216174
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.277-5021A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216174 | ||||||
| chr10:216184
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.277-5011C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216184 | ||||||
| chr10:216398
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-4797C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216398 | ||||||
| chr10:216503
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.277-4692G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216503 | ||||||
| chr10:216514
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.277-4681T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216514 | ||||||
| chr10:216627
|
G | T | 1 | a0001c0001t0001g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.277-4568G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216627 | ||||||
| chr10:216699
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.277-4496A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216699 | ||||||
| chr10:216721
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.277-4474A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216721 | ||||||
| chr10:216729
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-4466T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216729 | ||||||
| chr10:216914
|
C | T | 77 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0190others(74): Show | 77 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.277-4281C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216914 | ||||||
| chr10:216915
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-4280A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 216915 | ||||||
| chr10:217118
|
T | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0258 | 2 | HG01346.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.277-4077T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217118 | ||||||
| chr10:217125
|
C | CTT | 304 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.277-4069_277-4068i others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 217125 | |||||
| chr10:217190
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.277-4005C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217190 | ||||||
| chr10:217229
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-3966A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217229 | ||||||
| chr10:217319
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.277-3876G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217319 | ||||||
| chr10:217325
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.277-3870G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217325 | ||||||
| chr10:217378
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.277-3817C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217378 | ||||||
| chr10:217429
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.277-3766G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217429 | ||||||
| chr10:217514
|
C | CA | 8 | a0001c0001t0001g0110a0001c0001t0001g0136a0001c0001t0001g0138others(5): Show | 9 | HG02055.hp1 HG02615.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-3664dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 217514 | |||||
| chr10:217580
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-3615G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217580 | ||||||
| chr10:217597
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.277-3598A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217597 | ||||||
| chr10:217624
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.277-3571G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217624 | ||||||
| chr10:217711
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.277-3484A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217711 | ||||||
| chr10:217724
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-3471G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217724 | ||||||
| chr10:217871
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0338 | 2 | HG02965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.277-3324A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 217871 | ||||||
| chr10:218477
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-2718C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 218477 | ||||||
| chr10:218579
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.277-2616T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 218579 | ||||||
| chr10:218741
|
A | T | 2 | a0001c0002t0001g0159a0001c0002t0001g0178 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.277-2454A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 218741 | ||||||
| chr10:218981
|
G | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-2214G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 218981 | ||||||
| chr10:219102
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.277-2093A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 219102 | ||||||
| chr10:219412
|
T | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0281a0001c0001t0001g0286others(1): Show | 4 | HG01069.hp2 HG01109.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-1783T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 219412 | ||||||
| chr10:219554
|
A | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0001g0268 | 3 | HG00639.hp1 HG01169.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.277-1641A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 219554 | ||||||
| chr10:219580
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.277-1615A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 219580 | ||||||
| chr10:219643
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.277-1552C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 219643 | ||||||
| chr10:220078
|
G | T | 1 | a0001c0001t0001g0331 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.277-1117G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220078 | ||||||
| chr10:220116
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.277-1079T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220116 | ||||||
| chr10:220176
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.277-1019A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220176 | ||||||
| chr10:220198
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.277-997T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220198 | ||||||
| chr10:220433
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0197 | 2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-762T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220433 | ||||||
| chr10:220694
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.277-501A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220694 | ||||||
| chr10:220710
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.277-485C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220710 | ||||||
| chr10:220719
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.277-476G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220719 | ||||||
| chr10:220735
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0129 | 2 | HG02165.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.277-460A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | chr10 | 220735 | ||||||
| chr10:220747
|
T | TATTACTA others(15): Show |
1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.277-447_277-426dup others(22): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 220747 | |||||
| chr10:220787
|
T | TTA | 4 | a0001c0001t0001g0053a0001c0001t0001g0284a0001c0001t0001g0285others(1): Show | 4 | HG03486.hp1 HG03540.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-396_277-395dup others(2): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 220787 | |||||
| chr10:221371
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.438+15G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221371 | ||||||
| chr10:221457
|
A | G | 1 | a0001c0002t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.438+101A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221457 | ||||||
| chr10:221550
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.438+194A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221550 | ||||||
| chr10:221558
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.438+202T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221558 | ||||||
| chr10:221640
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.438+284A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221640 | ||||||
| chr10:221890
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.438+534A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221890 | ||||||
| chr10:221991
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.438+635C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 221991 | ||||||
| chr10:222294
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.438+938T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222294 | ||||||
| chr10:222324
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0197 | 2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438+968C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222324 | ||||||
| chr10:222430
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.438+1074A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222430 | ||||||
| chr10:222468
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.438+1112G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222468 | ||||||
| chr10:222577
|
G | A | 76 | a0001c0001t0001g0136a0001c0001t0001g0184a0001c0001t0001g0188others(73): Show | 76 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.438+1221G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222577 | ||||||
| chr10:222652
|
T | G | 82 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0027others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.438+1296T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222652 | ||||||
| chr10:222893
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1537C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222893 | ||||||
| chr10:222900
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.438+1544G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222900 | ||||||
| chr10:222982
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.438+1626G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 222982 | ||||||
| chr10:223032
|
C | CT | 37 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(34): Show | 38 | HG00597.hp1 HG00733.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.438+1689dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 223032 | |||||
| chr10:223032
|
CT | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.438+1689delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 223032 | |||||
| chr10:223074
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.438+1718G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223074 | ||||||
| chr10:223132
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.438+1776T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223132 | ||||||
| chr10:223133
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+1777G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223133 | ||||||
| chr10:223161
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.438+1805C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223161 | ||||||
| chr10:223299
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.438+1943A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223299 | ||||||
| chr10:223671
|
A | G | 1 | a0001c0001t0001g0329 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.438+2315A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223671 | ||||||
| chr10:223730
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.438+2374G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223730 | ||||||
| chr10:223755
|
C | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.438+2399C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223755 | ||||||
| chr10:223840
|
T | G | 82 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0027others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.438+2484T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 223840 | ||||||
| chr10:224223
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.438+2867T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 224223 | ||||||
| chr10:224270
|
A | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0066 | 3 | NA18942.hp2 NA18955.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.438+2914A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 224270 | ||||||
| chr10:224493
|
ACTTTTAC others(8): Show |
A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.438+3140_438+3154d others(17): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 224493 | |||||
| chr10:224532
|
G | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(2): Show | 5 | HG00558.hp2 NA18940.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3176G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 224532 | ||||||
| chr10:224673
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.438+3317A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 224673 | ||||||
| chr10:224788
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.438+3432C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 224788 | ||||||
| chr10:225021
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.438+3665A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225021 | ||||||
| chr10:225077
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.438+3721A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225077 | ||||||
| chr10:225139
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.438+3783T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225139 | ||||||
| chr10:225342
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.438+3986T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225342 | ||||||
| chr10:225354
|
T | TA | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+3998_438+3999i others(3): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225354 | ||||||
| chr10:225356
|
T | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+4000T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225356 | ||||||
| chr10:225358
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+4002A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225358 | ||||||
| chr10:225362
|
G | GTGTT | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.438+4008_438+4011d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 225362 | |||||
| chr10:225362
|
G | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+4006G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225362 | ||||||
| chr10:225489
|
C | T | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 7 | NA18941.hp1 NA18945.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+4133C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225489 | ||||||
| chr10:225533
|
A | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(213): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.438+4177A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225533 | ||||||
| chr10:225752
|
G | A | 8 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 8 | HG02040.hp2 HG02056.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+4396G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 225752 | ||||||
| chr10:226049
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.438+4693G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226049 | ||||||
| chr10:226113
|
G | C | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 7 | NA18941.hp1 NA18945.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+4757G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226113 | ||||||
| chr10:226224
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(212): Show | 216 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.438+4868C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226224 | ||||||
| chr10:226272
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.438+4916C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226272 | ||||||
| chr10:226315
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.438+4959A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226315 | ||||||
| chr10:226388
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.438+5032T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226388 | ||||||
| chr10:226443
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.438+5087T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226443 | ||||||
| chr10:226519
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.438+5163T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226519 | ||||||
| chr10:226610
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.438+5254G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226610 | ||||||
| chr10:226672
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.438+5316G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226672 | ||||||
| chr10:226693
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+5337G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226693 | ||||||
| chr10:226956
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.438+5600G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 226956 | ||||||
| chr10:227142
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.438+5786A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227142 | ||||||
| chr10:227262
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.438+5906T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227262 | ||||||
| chr10:227332
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.438+5976G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227332 | ||||||
| chr10:227349
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.438+5993C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227349 | ||||||
| chr10:227404
|
A | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(38): Show | 42 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.438+6048A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227404 | ||||||
| chr10:227435
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0126 | 3 | NA18978.hp1 NA19002.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.438+6079C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227435 | ||||||
| chr10:227505
|
TTGAGCCA others(7): Show |
T | 72 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.438+6152_438+6165d others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 227505 | |||||
| chr10:227600
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0123 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.438+6244C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227600 | ||||||
| chr10:227782
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.438+6426G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227782 | ||||||
| chr10:227975
|
A | G | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.438+6619A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 227975 | ||||||
| chr10:228163
|
A | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0116others(1): Show | 4 | NA18967.hp2 NA18970.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+6807A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228163 | ||||||
| chr10:228222
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.438+6866C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228222 | ||||||
| chr10:228284
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.438+6928A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228284 | ||||||
| chr10:228405
|
G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+7049G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228405 | ||||||
| chr10:228684
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0006g0172 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.438+7328T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228684 | ||||||
| chr10:228735
|
T | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(213): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.438+7379T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228735 | ||||||
| chr10:228754
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0126 | 3 | NA18978.hp1 NA19002.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.438+7398A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 228754 | ||||||
| chr10:229217
|
A | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0212a0001c0001t0001g0222others(1): Show | 4 | HG01123.hp2 HG01346.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-7621A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 229217 | ||||||
| chr10:229220
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-7618T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 229220 | ||||||
| chr10:229547
|
C | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0295others(2): Show | 5 | HG00558.hp2 NA18940.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-7291C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 229547 | ||||||
| chr10:229935
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0102others(3): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-6903A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 229935 | ||||||
| chr10:229947
|
C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-6891C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 229947 | ||||||
| chr10:230054
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0106others(68): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.439-6784A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230054 | ||||||
| chr10:230088
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-6750A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230088 | ||||||
| chr10:230203
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.439-6635G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230203 | ||||||
| chr10:230263
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0106others(68): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.439-6575A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230263 | ||||||
| chr10:230325
|
TAGCCC | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-6509_439-6505d others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230325 | |||||
| chr10:230421
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.439-6417T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230421 | ||||||
| chr10:230422
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.439-6416G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230422 | ||||||
| chr10:230427
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.439-6411C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230427 | ||||||
| chr10:230472
|
C | CA | 18 | a0001c0001t0001g0152a0001c0001t0001g0339a0001c0002t0001g0105others(15): Show | 18 | HG01074.hp2 HG01192.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.439-6337dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAA | C | 10 | a0001c0001t0001g0049a0001c0001t0001g0251a0001c0001t0001g0313others(7): Show | 10 | HG00609.hp1 HG01952.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.439-6338_439-6337d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAAA | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(64): Show | 67 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.439-6339_439-6337d others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAAAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.439-6340_439-6337d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAAAAA | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.439-6341_439-6337d others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0253 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.439-6347_439-6337d others(13): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230472
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-6348_439-6337d others(14): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 230472 | |||||
| chr10:230494
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.439-6344A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230494 | ||||||
| chr10:230499
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0147 | 3 | NA19056.hp2 NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.439-6339A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230499 | ||||||
| chr10:230503
|
T | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-6335T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230503 | ||||||
| chr10:230512
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-6326C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230512 | ||||||
| chr10:230861
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.439-5977G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 230861 | ||||||
| chr10:231292
|
A | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(79): Show | 82 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.439-5546A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 231292 | ||||||
| chr10:231390
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(216): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.439-5448T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 231390 | ||||||
| chr10:231830
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-5008C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 231830 | ||||||
| chr10:231900
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-4938T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 231900 | ||||||
| chr10:231954
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-4884G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 231954 | ||||||
| chr10:232020
|
G | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0106others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.439-4818G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232020 | ||||||
| chr10:232067
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.439-4771A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232067 | ||||||
| chr10:232274
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.439-4564G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232274 | ||||||
| chr10:232559
|
C | T | 1 | a0001c0002t0001g0153 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-4279C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232559 | ||||||
| chr10:232799
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-4039A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232799 | ||||||
| chr10:232871
|
C | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-3967C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232871 | ||||||
| chr10:232887
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-3951C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232887 | ||||||
| chr10:232914
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.439-3924G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 232914 | ||||||
| chr10:233041
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439-3797C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233041 | ||||||
| chr10:233178
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.439-3660C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233178 | ||||||
| chr10:233222
|
T | TA | 69 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.439-3612dupA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 233222 | |||||
| chr10:233251
|
A | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.439-3587A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233251 | ||||||
| chr10:233308
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.439-3530C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233308 | ||||||
| chr10:233347
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-3491A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233347 | ||||||
| chr10:233365
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.439-3473C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233365 | ||||||
| chr10:233412
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-3426T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233412 | ||||||
| chr10:233427
|
C | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-3411C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233427 | ||||||
| chr10:233499
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.439-3339A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233499 | ||||||
| chr10:233556
|
G | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.439-3282G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233556 | ||||||
| chr10:233557
|
G | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0035others(66): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.439-3281G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233557 | ||||||
| chr10:233774
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.439-3064C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233774 | ||||||
| chr10:233915
|
C | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.439-2923C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233915 | ||||||
| chr10:233929
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.439-2909T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 233929 | ||||||
| chr10:234013
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.439-2825G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234013 | ||||||
| chr10:234229
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.439-2609A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234229 | ||||||
| chr10:234255
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-2583G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234255 | ||||||
| chr10:234372
|
A | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG00609.hp1 HG01496.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-2466A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234372 | ||||||
| chr10:234431
|
T | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.439-2407T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234431 | ||||||
| chr10:234459
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.439-2379C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234459 | ||||||
| chr10:234460
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077 | 3 | NA18962.hp2 NA18973.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.439-2378G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234460 | ||||||
| chr10:234696
|
TCTC | T | 4 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-2139_439-2137d others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234696 | |||||
| chr10:234747
|
ATCTCCAG others(3): Show |
A | 1 | a0001c0001t0001g0281 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.439-2087_439-2078d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234747 | |||||
| chr10:234764
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.439-2074G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 234764 | ||||||
| chr10:234982
|
A | ATG | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.439-1829_439-1828d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTATGT others(1): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0001g0268 | 3 | HG00639.hp1 HG01169.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.439-1853_439-1852i others(10): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTG | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(101): Show | 105 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.439-1831_439-1828d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTGTG | 14 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG01243.hp2 HG01257.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-1833_439-1828d others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTGTGT others(3): Show |
7 | a0001c0001t0001g0046a0001c0001t0001g0074a0001c0001t0001g0075others(4): Show | 7 | HG00558.hp1 HG03492.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-1837_439-1828d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTGTGT others(5): Show |
49 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0027others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.439-1839_439-1828d others(14): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTGTGT others(7): Show |
17 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0037others(14): Show | 17 | HG00639.hp2 HG01123.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.439-1841_439-1828d others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
A | ATGTGTGT others(9): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0252a0001c0001t0001g0259others(1): Show | 4 | HG00438.hp1 HG02132.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-1843_439-1828d others(18): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
ATG | A | 29 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(26): Show | 30 | HG00733.hp1 HG01074.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.439-1829_439-1828d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:234982
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0010g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.439-1837_439-1828d others(12): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 234982 | |||||
| chr10:235078
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.439-1760C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235078 | ||||||
| chr10:235201
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.439-1637A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235201 | ||||||
| chr10:235208
|
AAATTT | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-1626_439-1622d others(7): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 235208 | |||||
| chr10:235259
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.439-1579T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235259 | ||||||
| chr10:235264
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.439-1574G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235264 | ||||||
| chr10:235307
|
A | G | 99 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.439-1531A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235307 | ||||||
| chr10:235374
|
CAG | C | 4 | a0001c0001t0001g0330a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG00673.hp2 NA18945.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-1460_439-1459d others(4): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 235374 | |||||
| chr10:235523
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.439-1315G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235523 | ||||||
| chr10:235542
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.439-1296G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235542 | ||||||
| chr10:235688
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.439-1150G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235688 | ||||||
| chr10:235763
|
A | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.439-1075A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235763 | ||||||
| chr10:235770
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(224): Show | 228 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.439-1068G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235770 | ||||||
| chr10:235862
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.439-976A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235862 | ||||||
| chr10:235871
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.439-967T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235871 | ||||||
| chr10:235938
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439-900A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235938 | ||||||
| chr10:235956
|
A | C | 98 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.439-882A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235956 | ||||||
| chr10:235972
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.439-866T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235972 | ||||||
| chr10:235986
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.439-852A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 235986 | ||||||
| chr10:236081
|
A | C | 1 | a0001c0002t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.439-757A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236081 | ||||||
| chr10:236117
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.439-721T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236117 | ||||||
| chr10:236196
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.439-642A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236196 | ||||||
| chr10:236211
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.439-627C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236211 | ||||||
| chr10:236233
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.439-605C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236233 | ||||||
| chr10:236271
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG00140.hp2 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.439-567T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236271 | ||||||
| chr10:236381
|
T | G | 4 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0325others(1): Show | 4 | HG01952.hp1 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-457T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236381 | ||||||
| chr10:236580
|
CAAGAA | C | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0300 | 3 | HG03486.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.439-250_439-246del others(5): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 236580 | |||||
| chr10:236619
|
A | T | 1 | a0001c0001t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.439-219A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236619 | ||||||
| chr10:236713
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.439-125G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236713 | ||||||
| chr10:236741
|
GCATACTA others(3): Show |
G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-96_439-87delCA others(8): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | chr10 | 236741 | ||||||
| chr10:236816
|
TTTA | T | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-19_439-17delAT others(1): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 236816 | |||||
| chr10:236948
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.516+33C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 236948 | ||||||
| chr10:236957
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.516+42C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 236957 | ||||||
| chr10:236995
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+80G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 236995 | ||||||
| chr10:237020
|
A | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0310 | 2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.516+105A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237020 | ||||||
| chr10:237070
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.516+155A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237070 | ||||||
| chr10:237118
|
G | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.516+203G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237118 | ||||||
| chr10:237250
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.516+335A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237250 | ||||||
| chr10:237369
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.517-216G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237369 | ||||||
| chr10:237434
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.517-151G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237434 | ||||||
| chr10:237557
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.517-28T>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 5/14 | chr10 | 237557 | ||||||
| chr10:238363
|
C | CT | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 44 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.609+697dupT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr10 | 238363 | |||||
| chr10:238368
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.609+691T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238368 | ||||||
| chr10:238393
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+716G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238393 | ||||||
| chr10:238423
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.609+746C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238423 | ||||||
| chr10:238547
|
G | A | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+870G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238547 | ||||||
| chr10:238573
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02559.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.610-865G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238573 | ||||||
| chr10:238654
|
C | A | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610-784C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238654 | ||||||
| chr10:238802
|
G | A | 1 | a0001c0001t0004g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.610-636G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238802 | ||||||
| chr10:238921
|
C | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.610-517C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238921 | ||||||
| chr10:238998
|
T | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.610-440T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 238998 | ||||||
| chr10:239047
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.610-391T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239047 | ||||||
| chr10:239056
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.610-382C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239056 | ||||||
| chr10:239062
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.610-376T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239062 | ||||||
| chr10:239122
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.610-316G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239122 | ||||||
| chr10:239123
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.610-315C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239123 | ||||||
| chr10:239173
|
C | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.610-265C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239173 | ||||||
| chr10:239224
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.610-214G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239224 | ||||||
| chr10:239260
|
T | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.610-178T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239260 | ||||||
| chr10:239369
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.610-69G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 6/14 | chr10 | 239369 | ||||||
| chr10:239539
|
G | GTGT | 70 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 71 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.697+15_697+16insGT others(1): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 239539 | |||||
| chr10:239539
|
G | GTGTT | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.697+15_697+16insGT others(2): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 239539 | |||||
| chr10:239866
|
A | C | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.698-190A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 7/14 | chr10 | 239866 | ||||||
| chr10:240009
|
G | A | 11 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0198others(8): Show | 11 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.698-47G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 7/14 | chr10 | 240009 | ||||||
| chr10:240281
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.753+170G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 8/14 | chr10 | 240281 | ||||||
| chr10:240391
|
C | T | 1 | a0001c0002t0001g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.753+280C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 8/14 | chr10 | 240391 | ||||||
| chr10:240434
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0066 | 2 | NA18955.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.753+323G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 8/14 | chr10 | 240434 | ||||||
| chr10:240803
|
C | T | 2 | a0001c0001t0001g0249a0001c0002t0001g0241 | 2 | HG02040.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.754-90C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 8/14 | chr10 | 240803 | ||||||
| chr10:240853
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-40A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 8/14 | chr10 | 240853 | ||||||
| chr10:241572
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.832-449C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241572 | ||||||
| chr10:241725
|
G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-296G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241725 | ||||||
| chr10:241727
|
A | AGCT | 43 | a0001c0001t0001g0017a0001c0001t0001g0152a0001c0001t0001g0163others(40): Show | 44 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.832-289_832-287dup others(3): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 241727 | |||||
| chr10:241780
|
G | A | 3 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0175 | 3 | HG02055.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.832-241G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241780 | ||||||
| chr10:241800
|
T | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0159others(2): Show | 5 | HG02055.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-221T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241800 | ||||||
| chr10:241824
|
G | A | 18 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0047others(15): Show | 18 | HG02071.hp2 HG02080.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.832-197G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241824 | ||||||
| chr10:241871
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.832-150A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 9/14 | chr10 | 241871 | ||||||
| chr10:242164
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0335 | 3 | HG03927.hp1 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.950+25G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242164 | ||||||
| chr10:242168
|
A | G | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+29A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242168 | ||||||
| chr10:242244
|
G | GAA | 93 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.950+114_950+115dup others(2): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 242244 | |||||
| chr10:242254
|
A | C | 3 | a0001c0002t0001g0153a0001c0002t0001g0171a0001c0002t0001g0179 | 3 | NA18941.hp2 NA18963.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.950+115A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242254 | ||||||
| chr10:242255
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.950+116C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242255 | ||||||
| chr10:242427
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.950+288T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242427 | ||||||
| chr10:242474
|
TAGTTGCT others(2): Show |
T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0335 | 3 | HG03927.hp1 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.950+338_950+346del others(9): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 242474 | |||||
| chr10:242514
|
T | C | 4 | a0001c0002t0001g0238a0001c0002t0001g0239a0001c0002t0001g0240others(1): Show | 4 | HG01192.hp1 HG02258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+375T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242514 | ||||||
| chr10:242567
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.950+428G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242567 | ||||||
| chr10:242618
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+479T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242618 | ||||||
| chr10:242910
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG00639.hp2 HG03834.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.950+771C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 242910 | ||||||
| chr10:243006
|
AT | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.950+872delT | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 243006 | |||||
| chr10:243091
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.950+952G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 243091 | ||||||
| chr10:243234
|
G | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0294 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.950+1095G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 243234 | ||||||
| chr10:243910
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.950+1771G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 243910 | ||||||
| chr10:244071
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+1932A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 244071 | ||||||
| chr10:244096
|
TTTTTCCT others(7): Show |
T | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0300 | 3 | HG03486.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.950+1958_950+1971d others(16): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 244096 | ||||||
| chr10:244330
|
GA | G | 4 | a0001c0001t0001g0282a0001c0001t0001g0287a0001c0001t0001g0309others(1): Show | 4 | HG00642.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+2199delA | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 244330 | |||||
| chr10:244629
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.951-2137C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 244629 | ||||||
| chr10:244789
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0264a0001c0001t0001g0266others(1): Show | 4 | HG00639.hp1 HG01169.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-1977C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 244789 | ||||||
| chr10:244790
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.951-1976G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 244790 | ||||||
| chr10:245194
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0030others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.951-1572T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245194 | ||||||
| chr10:245330
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.951-1436G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245330 | ||||||
| chr10:245568
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.951-1198C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245568 | ||||||
| chr10:245592
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.951-1174C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245592 | ||||||
| chr10:245593
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.951-1173A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245593 | ||||||
| chr10:245661
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-1105C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245661 | ||||||
| chr10:245832
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.951-934A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245832 | ||||||
| chr10:245902
|
T | C | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.951-864T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245902 | ||||||
| chr10:245928
|
C | T | 70 | a0001c0001t0001g0135a0001c0001t0001g0184a0001c0001t0001g0188others(67): Show | 70 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.951-838C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245928 | ||||||
| chr10:245930
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0269 | 2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.951-836G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245930 | ||||||
| chr10:245939
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.951-827T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245939 | ||||||
| chr10:245953
|
T | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0082others(69): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.951-813T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245953 | ||||||
| chr10:245980
|
T | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0097others(2): Show | 5 | HG01891.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-786T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 245980 | ||||||
| chr10:246033
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.951-733A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 246033 | ||||||
| chr10:246059
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.951-707G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 246059 | ||||||
| chr10:246171
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-595C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 246171 | ||||||
| chr10:246393
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.951-373A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 246393 | ||||||
| chr10:246690
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.951-76T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 10/14 | chr10 | 246690 | ||||||
| chr10:246987
|
C | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1158+14C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 11/14 | chr10 | 246987 | ||||||
| chr10:247824
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1227+358A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 247824 | ||||||
| chr10:247904
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1228-432A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 247904 | ||||||
| chr10:247923
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228-413C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 247923 | ||||||
| chr10:248184
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1228-152C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 248184 | ||||||
| chr10:248205
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1228-131T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 248205 | ||||||
| chr10:248225
|
T | C | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1228-111T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 248225 | ||||||
| chr10:248254
|
A | G | 4 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0325others(1): Show | 4 | HG01952.hp1 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-82A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 12/14 | chr10 | 248254 | ||||||
| chr10:248720
|
ATGACACC others(8): Show |
A | 1 | a0001c0002t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1500+114_1500+128d others(17): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 248720 | |||||
| chr10:248753
|
A | T | 1 | a0001c0002t0001g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1500+145A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 13/14 | chr10 | 248753 | ||||||
| chr10:248756
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1501-147A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 13/14 | chr10 | 248756 | ||||||
| chr10:248888
|
G | C | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1501-15G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 13/14 | chr10 | 248888 | ||||||
| chr10:249157
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1686+69G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249157 | ||||||
| chr10:249394
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0078 | 2 | HG00280.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1686+306T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249394 | ||||||
| chr10:249600
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1686+512A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249600 | ||||||
| chr10:249630
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0062 | 3 | HG01123.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1686+542C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249630 | ||||||
| chr10:249635
|
C | T | 30 | a0001c0002t0001g0002a0001c0002t0001g0105a0001c0002t0001g0146others(27): Show | 31 | HG00597.hp1 HG00733.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1686+547C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249635 | ||||||
| chr10:249644
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1686+556T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249644 | ||||||
| chr10:249682
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1686+594C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249682 | ||||||
| chr10:249683
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1686+595G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249683 | ||||||
| chr10:249822
|
A | T | 1 | a0001c0002t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1686+734A>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249822 | ||||||
| chr10:249874
|
G | A | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686+786G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249874 | ||||||
| chr10:249970
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1686+882C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 249970 | ||||||
| chr10:250040
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG00639.hp2 HG03834.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686+952T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250040 | ||||||
| chr10:250052
|
C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0022others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686+964C>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250052 | ||||||
| chr10:250068
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1686+980T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250068 | ||||||
| chr10:250116
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00735.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1686+1028C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250116 | ||||||
| chr10:250281
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1686+1193A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250281 | ||||||
| chr10:250400
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1686+1312T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250400 | ||||||
| chr10:250499
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1411A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250499 | ||||||
| chr10:250501
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1413A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250501 | ||||||
| chr10:250505
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1417C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250505 | ||||||
| chr10:250506
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1418T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250506 | ||||||
| chr10:250509
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1421T>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250509 | ||||||
| chr10:250510
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1422G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250510 | ||||||
| chr10:250511
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1423A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250511 | ||||||
| chr10:250512
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1424G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250512 | ||||||
| chr10:250515
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1427G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250515 | ||||||
| chr10:250516
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1428A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250516 | ||||||
| chr10:250520
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1432C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250520 | ||||||
| chr10:250522
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+1434C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250522 | ||||||
| chr10:250587
|
A | C | 1 | a0001c0001t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1686+1499A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250587 | ||||||
| chr10:250690
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1686+1602A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250690 | ||||||
| chr10:250701
|
C | A | 1 | a0001c0001t0001g0334 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1686+1613C>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250701 | ||||||
| chr10:250765
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1687-1583C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250765 | ||||||
| chr10:250775
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1687-1573A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250775 | ||||||
| chr10:250973
|
A | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0269 | 2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1687-1375A>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 250973 | ||||||
| chr10:251085
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1687-1263T>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251085 | ||||||
| chr10:251441
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1687-907G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251441 | ||||||
| chr10:251460
|
G | A | 3 | a0001c0002t0001g0165a0001c0002t0001g0237a0001c0003t0001g0167 | 3 | HG00597.hp1 NA18967.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1687-888G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251460 | ||||||
| chr10:251614
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1687-734G>A | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251614 | ||||||
| chr10:251693
|
A | G | 122 | a0001c0001t0001g0135a0001c0001t0001g0152a0001c0001t0001g0163others(119): Show | 123 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.1687-655A>G | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251693 | ||||||
| chr10:251747
|
G | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-601G>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251747 | ||||||
| chr10:251890
|
GAAGT | G | 42 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0170others(39): Show | 43 | HG00597.hp1 HG00733.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1687-457_1687-454d others(6): Show |
ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251890 | ||||||
| chr10:251913
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1687-435C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 251913 | ||||||
| chr10:252053
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1687-295G>C | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 252053 | ||||||
| chr10:252306
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1687-42C>T | ZMYND11 | ENSG00000015171.21 | transcript | ENST00000381604.9 | protein_coding | 14/14 | chr10 | 252306 |