Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4603 |
|---|---|
| ensemblid | ENSG00000185697.17 |
| hgncid | 7547 |
| symbol | MYBL1 |
| name | MYB proto-oncogene like 1 |
| refseq_nuc | NM_001080416.4 |
| refseq_prot | NP_001073885.1 |
| ensembl_nuc | ENST00000522677.8 |
| ensembl_prot | ENSP00000429633.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 66562175 |
| end | 66613218 |
| strand | - |
| ver | v1.2 |
| region | chr8:66562175-66613218 |
| region5000 | chr8:66557175-66618218 |
| regionname0 | MYBL1_chr8_66562175_66613218 |
| regionname5000 | MYBL1_chr8_66557175_66618218 |
| 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 | 752 | 234 | 77 | 23 | 83 | 14 | 35 | 60 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0002 | 0/0 | 752 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0003 | 0/0 | 752 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0004 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2259 | 231 | 74 | 23 | 83 | 14 | 35 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| c0002 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| c0003 | 0/0 | 2259 | 2 | 0 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| c0004 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| c0005 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| 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 | 2903 | 159 | 33 | 23 | 62 | 13 | 26 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0002 | 0/0 | 2903 | 24 | 4 | 0 | 14 | 0 | 6 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0003 | 0/0 | 2903 | 22 | 20 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0004 | 0/0 | 2899 | 6 | 6 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0005 | 0/0 | 2903 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0006 | 0/0 | 2903 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0007 | 0/0 | 2903 | 4 | 0 | 1 | 0 | 1 | 2 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0008 | 0/0 | 2903 | 4 | 0 | 0 | 4 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0009 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0010 | 0/0 | 2903 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0011 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0012 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0013 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0014 | 0/0 | 2903 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| t0015 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2259 | 231 | 74 | 23 | 83 | 14 | 35 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0002 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0002c0003 | 0/0 | 2259 | 2 | 0 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0003c0005 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0004c0004 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5161 | 158 | 33 | 22 | 62 | 13 | 26 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0002 | 0/0 | 5161 | 24 | 4 | 0 | 14 | 0 | 6 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0003 | 0/0 | 5161 | 16 | 16 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0004 | 0/0 | 5157 | 6 | 6 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0005 | 0/0 | 5161 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0006 | 0/0 | 5161 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0007 | 0/0 | 5161 | 4 | 0 | 1 | 0 | 1 | 2 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0008 | 0/0 | 5161 | 4 | 0 | 0 | 4 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0009 | 0/0 | 5161 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0010 | 0/0 | 5161 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0011 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0012 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0013 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0014 | 0/0 | 5161 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0001t0015 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0001c0002t0003 | 0/0 | 5161 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0002c0003t0003 | 0/0 | 5161 | 2 | 0 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0003c0005t0001 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| a0004c0004t0003 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | copy fasta | chr8 | 66557175 | 66618218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0003c0005t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0004c0004t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0087 | EUR | FIN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0084 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01081 | hp1 | a0003 | c0005 | t0001 | g0140 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0089 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02132 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02165 | hp2 | a0001 | c0001 | t0009 | g0104 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02523 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02683 | hp1 | a0002 | c0003 | t0003 | g0025 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02809 | hp1 | a0004 | c0004 | t0003 | g0035 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0011 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0065 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0086 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0090 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03492 | hp2 | a0001 | c0001 | t0014 | g0131 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0222 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19011 | hp2 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ASW | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ASW | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | GIH | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | GIH | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0066 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0231 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0209 | REF | REF | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66566196
|
T | G | 1 | a0002 | 2 | HG02523.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.1998A>C | p.Glu666Asp | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/16 | 2378/5161 | 1998/2259 | 666/752 | chr8 | 66566196 | ||
| chr8:66573455
|
A | G | 1 | a0003 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1522T>C | p.Phe508Leu | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/16 | 1902/5161 | 1522/2259 | 508/752 | chr8 | 66573455 | ||
| chr8:66593128
|
A | T | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.754T>A | p.Phe252Ile | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 7/16 | 1134/5161 | 754/2259 | 252/752 | chr8 | 66593128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66592542
|
T | C | 2 | a0001c0002a0004c0004 | 4 | HG02109.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.765A>G | p.Gln255Gln | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/16 | 1145/5161 | 765/2259 | 255/752 | chr8 | 66592542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66562694
|
C | A | 1 | a0001c0001t0014 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 2003 | chr8 | 66562694 | |||||
| chr8:66562741
|
G | C | 1 | a0001c0001t0006 | 5 | HG02615.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1956C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1956 | chr8 | 66562741 | |||||
| chr8:66562854
|
CTATT | C | 1 | a0001c0001t0004 | 6 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1839_*1842delAATA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1839 | chr8 | 66562854 | |||||
| chr8:66562937
|
A | T | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1760 | chr8 | 66562937 | |||||
| chr8:66562968
|
T | C | 1 | a0001c0001t0015 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1729 | chr8 | 66562968 | |||||
| chr8:66563066
|
A | G | 7 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(4): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1631T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1631 | chr8 | 66563066 | |||||
| chr8:66563097
|
T | C | 1 | a0001c0001t0008 | 4 | HG00408.hp1 HG02015.hp2 NA18970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1600A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1600 | chr8 | 66563097 | |||||
| chr8:66563815
|
T | C | 1 | a0001c0001t0002 | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*882A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 882 | chr8 | 66563815 | |||||
| chr8:66563836
|
T | C | 1 | a0001c0001t0009 | 2 | HG02165.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*861A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 861 | chr8 | 66563836 | |||||
| chr8:66564048
|
G | T | 1 | a0001c0001t0007 | 4 | HG00323.hp2 HG01433.hp1 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*649C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 649 | chr8 | 66564048 | |||||
| chr8:66612993
|
C | T | 1 | a0001c0001t0012 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-155G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 155 | chr8 | 66612993 | |||||
| chr8:66613163
|
C | T | 1 | a0001c0001t0011 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-325G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 325 | chr8 | 66613163 | |||||
| chr8:66613179
|
G | A | 1 | a0001c0001t0010 | 2 | HG03453.hp2 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-341C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 341 | chr8 | 66613179 | |||||
| chr8:66613198
|
C | T | 1 | a0001c0001t0005 | 5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-360G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 360 | chr8 | 66613198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66565413
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2131-588C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565413 | ||||||
| chr8:66565451
|
TTGCCAAA others(15): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2130+591_2130+612d others(24): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565451 | ||||||
| chr8:66565550
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2130+514T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565550 | ||||||
| chr8:66565630
|
GA | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(226): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2130+433delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565630 | ||||||
| chr8:66566323
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0224 | 2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1951-80C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566323 | ||||||
| chr8:66566501
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1950+183T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566501 | ||||||
| chr8:66566663
|
C | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1950+21G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566663 | ||||||
| chr8:66566863
|
A | G | 1 | a0003c0005t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1845+13T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 13/15 | chr8 | 66566863 | ||||||
| chr8:66567133
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1729-141T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567133 | ||||||
| chr8:66567410
|
C | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1729-418G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567410 | ||||||
| chr8:66567526
|
A | AGAGT | 3 | a0001c0001t0006g0003a0001c0001t0006g0057a0001c0001t0006g0058 | 4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729-535_1729-534i others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | ||||||
| chr8:66567526
|
A | AGT | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1729-536_1729-535d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | ||||||
| chr8:66567526
|
A | AGTGT | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1729-538_1729-535d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | ||||||
| chr8:66567526
|
AGT | A | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-536_1729-535d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | ||||||
| chr8:66567528
|
T | A | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(30): Show | 36 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1729-536A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567528 | ||||||
| chr8:66567530
|
T | A | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-538A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567530 | ||||||
| chr8:66567565
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0054 | 2 | NA18961.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1729-573A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567565 | ||||||
| chr8:66567576
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0149 | 2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1729-584C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567576 | ||||||
| chr8:66567907
|
C | A | 1 | a0001c0001t0003g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1729-915G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567907 | ||||||
| chr8:66568042
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1729-1050C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568042 | ||||||
| chr8:66568046
|
C | CA | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00423.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1729-1055dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568046 | ||||||
| chr8:66568060
|
A | C | 1 | a0001c0001t0015g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1729-1068T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568060 | ||||||
| chr8:66568063
|
C | A | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-1071G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568063 | ||||||
| chr8:66568748
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1729-1756G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568748 | ||||||
| chr8:66568791
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1729-1799G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568791 | ||||||
| chr8:66568808
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1729-1816G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568808 | ||||||
| chr8:66568854
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1729-1862C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568854 | ||||||
| chr8:66569322
|
C | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1729-2330G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569322 | ||||||
| chr8:66569339
|
C | CT | 13 | a0001c0001t0002g0047a0001c0001t0003g0027a0001c0001t0003g0029others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1729-2348dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569339 | ||||||
| chr8:66569339
|
CT | C | 6 | a0001c0001t0001g0022a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG01884.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-2348delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569339 | ||||||
| chr8:66569582
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1729-2590G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569582 | ||||||
| chr8:66569726
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1729-2734T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569726 | ||||||
| chr8:66569781
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1728+2701C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569781 | ||||||
| chr8:66570065
|
G | A | 1 | a0001c0001t0006g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1728+2417C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570065 | ||||||
| chr8:66570111
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1728+2371A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570111 | ||||||
| chr8:66570312
|
CT | C | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1728+2169delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570312 | ||||||
| chr8:66570490
|
C | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1728+1992G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570490 | ||||||
| chr8:66570769
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1728+1713C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570769 | ||||||
| chr8:66570869
|
C | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1728+1613G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570869 | ||||||
| chr8:66571013
|
G | C | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1728+1469C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571013 | ||||||
| chr8:66571201
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1728+1281A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571201 | ||||||
| chr8:66571489
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1728+993A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571489 | ||||||
| chr8:66571665
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1728+817C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571665 | ||||||
| chr8:66571719
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1728+763T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571719 | ||||||
| chr8:66571729
|
A | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0050 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1728+753T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571729 | ||||||
| chr8:66571750
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1728+732C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571750 | ||||||
| chr8:66571813
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0005g0006a0001c0001t0005g0008others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+669C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571813 | ||||||
| chr8:66571892
|
GAA | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1728+588_1728+589d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571892 | ||||||
| chr8:66572080
|
G | T | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1728+402C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572080 | ||||||
| chr8:66572094
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1728+388A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572094 | ||||||
| chr8:66572147
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1728+335G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572147 | ||||||
| chr8:66572340
|
A | C | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1728+142T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572340 | ||||||
| chr8:66572382
|
A | C | 3 | a0001c0001t0004g0217a0001c0001t0004g0218a0001c0001t0004g0219 | 3 | HG02622.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1728+100T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572382 | ||||||
| chr8:66572864
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1614-268T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66572864 | ||||||
| chr8:66573060
|
C | A | 1 | a0002c0003t0003g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1613+304G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573060 | ||||||
| chr8:66573060
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA18957.hp2 NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1613+304G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573060 | ||||||
| chr8:66573151
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1613+213A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573151 | ||||||
| chr8:66573957
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1471-451A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573957 | ||||||
| chr8:66573970
|
C | CTGGCAAA others(5): Show |
7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-465_1471-464i others(14): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573970 | ||||||
| chr8:66573976
|
T | C | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-470A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573976 | ||||||
| chr8:66573977
|
G | A | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-471C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573977 | ||||||
| chr8:66573978
|
A | G | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-472T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573978 | ||||||
| chr8:66573979
|
T | A | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-473A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573979 | ||||||
| chr8:66573980
|
A | C | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-474T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573980 | ||||||
| chr8:66574077
|
T | C | 1 | a0001c0001t0006g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1471-571A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574077 | ||||||
| chr8:66574101
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1471-595T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574101 | ||||||
| chr8:66574149
|
G | C | 7 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(4): Show | 7 | NA18952.hp1 NA18957.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1471-643C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574149 | ||||||
| chr8:66574261
|
C | T | 1 | a0001c0001t0015g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1471-755G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574261 | ||||||
| chr8:66574662
|
T | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1471-1156A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574662 | ||||||
| chr8:66574680
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0070others(39): Show | 43 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1471-1174A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574680 | ||||||
| chr8:66574821
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1470+1186C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574821 | ||||||
| chr8:66574826
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1470+1181C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574826 | ||||||
| chr8:66575072
|
C | A | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1470+935G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575072 | ||||||
| chr8:66575267
|
AC | A | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1470+739delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575267 | ||||||
| chr8:66575319
|
T | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1470+688A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575319 | ||||||
| chr8:66575362
|
C | T | 3 | a0001c0001t0006g0003a0001c0001t0006g0057a0001c0001t0006g0058 | 4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1470+645G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575362 | ||||||
| chr8:66575363
|
G | A | 1 | a0001c0001t0008g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1470+644C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575363 | ||||||
| chr8:66575407
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1470+600T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575407 | ||||||
| chr8:66575473
|
A | C | 3 | a0001c0001t0006g0003a0001c0001t0006g0057a0001c0001t0006g0058 | 4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1470+534T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575473 | ||||||
| chr8:66575704
|
C | CA | 2 | a0001c0001t0001g0096a0001c0001t0001g0107 | 2 | NA18982.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1470+302dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575704 | ||||||
| chr8:66575741
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1470+266C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575741 | ||||||
| chr8:66575766
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1470+241C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575766 | ||||||
| chr8:66575816
|
A | G | 1 | a0001c0001t0003g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1470+191T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575816 | ||||||
| chr8:66575961
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1470+46C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575961 | ||||||
| chr8:66576575
|
T | C | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1102-200A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576575 | ||||||
| chr8:66576687
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1102-312G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576687 | ||||||
| chr8:66576689
|
T | G | 23 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(20): Show | 26 | HG02523.hp2 HG02683.hp1 HG02738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1102-314A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576689 | ||||||
| chr8:66576833
|
T | C | 1 | a0002c0003t0003g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1102-458A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576833 | ||||||
| chr8:66576926
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0192a0001c0001t0001g0201 | 3 | HG03490.hp2 HG04115.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1102-551G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576926 | ||||||
| chr8:66577134
|
G | A | 1 | a0002c0003t0003g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1102-759C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577134 | ||||||
| chr8:66577238
|
CAGG | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0001g0157 | 3 | HG00099.hp2 HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1102-866_1102-864d others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577238 | ||||||
| chr8:66577525
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0193 | 2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1102-1150G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577525 | ||||||
| chr8:66577582
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0109 | 2 | NA18992.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1102-1207A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577582 | ||||||
| chr8:66577603
|
TC | T | 21 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(18): Show | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.1102-1229delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577603 | ||||||
| chr8:66577634
|
G | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1102-1259C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577634 | ||||||
| chr8:66577995
|
A | G | 2 | a0001c0001t0003g0059a0001c0001t0003g0060 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1102-1620T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577995 | ||||||
| chr8:66578024
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1102-1649G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578024 | ||||||
| chr8:66578128
|
G | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1102-1753C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578128 | ||||||
| chr8:66578130
|
G | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1102-1755C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578130 | ||||||
| chr8:66578170
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1102-1795T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578170 | ||||||
| chr8:66578523
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0221 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1101+1610T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578523 | ||||||
| chr8:66578530
|
G | A | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1101+1603C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578530 | ||||||
| chr8:66578663
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1101+1470C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578663 | ||||||
| chr8:66578781
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101+1352T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578781 | ||||||
| chr8:66579010
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1101+1123G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579010 | ||||||
| chr8:66579014
|
A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(227): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1101+1119T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579014 | ||||||
| chr8:66579119
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0010g0231a0001c0001t0010g0232 | 3 | HG03130.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1101+1014A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579119 | ||||||
| chr8:66579239
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1101+894T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579239 | ||||||
| chr8:66579246
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1101+887T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579246 | ||||||
| chr8:66579259
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1101+874A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579259 | ||||||
| chr8:66579262
|
TA | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0200a0001c0001t0004g0129 | 3 | HG02895.hp2 NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1101+870delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579262 | ||||||
| chr8:66579263
|
A | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(220): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1101+870T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579263 | ||||||
| chr8:66579264
|
A | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 60 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.1101+869T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579264 | ||||||
| chr8:66579265
|
A | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1101+868T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579265 | ||||||
| chr8:66579266
|
A | T | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1101+867T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579266 | ||||||
| chr8:66579410
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0211 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1101+723T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579410 | ||||||
| chr8:66579635
|
C | T | 1 | a0001c0001t0015g0222 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1101+498G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579635 | ||||||
| chr8:66579648
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1101+485A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579648 | ||||||
| chr8:66579656
|
T | TA | 49 | a0001c0001t0001g0168a0001c0001t0002g0001a0001c0001t0002g0002others(46): Show | 53 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1101+476dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579656 | ||||||
| chr8:66579771
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1101+362A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579771 | ||||||
| chr8:66579979
|
AC | A | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101+153delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579979 | ||||||
| chr8:66580048
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1101+85A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66580048 | ||||||
| chr8:66580106
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1101+27A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66580106 | ||||||
| chr8:66580456
|
C | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-90G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580456 | ||||||
| chr8:66580702
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.868-336T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580702 | ||||||
| chr8:66580853
|
CTCT | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0151a0001c0001t0001g0178others(3): Show | 6 | HG01952.hp1 HG02155.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-490_868-488del others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580853 | ||||||
| chr8:66581270
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-904C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581270 | ||||||
| chr8:66581301
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.868-935T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581301 | ||||||
| chr8:66581414
|
C | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-1048G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581414 | ||||||
| chr8:66581550
|
G | A | 1 | a0001c0001t0010g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.868-1184C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581550 | ||||||
| chr8:66581566
|
C | T | 21 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(18): Show | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.868-1200G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581566 | ||||||
| chr8:66582139
|
C | T | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868-1773G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582139 | ||||||
| chr8:66582141
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.868-1775T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582141 | ||||||
| chr8:66582222
|
T | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-1856A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582222 | ||||||
| chr8:66582345
|
G | T | 10 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0038others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-1979C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582345 | ||||||
| chr8:66582354
|
T | C | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.868-1988A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582354 | ||||||
| chr8:66582438
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.868-2072G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582438 | ||||||
| chr8:66582514
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0070others(39): Show | 43 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.868-2148G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582514 | ||||||
| chr8:66582541
|
C | CA | 33 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0092others(30): Show | 36 | HG01433.hp1 HG01433.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.868-2176dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | ||||||
| chr8:66582541
|
C | CAA | 18 | a0001c0001t0002g0002a0001c0001t0002g0039a0001c0001t0002g0041others(15): Show | 19 | HG00408.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.868-2177_868-2176d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | ||||||
| chr8:66582541
|
C | CAAA | 9 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-2178_868-2176d others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | ||||||
| chr8:66582541
|
C | CAAAA | 5 | a0001c0001t0003g0032a0001c0001t0013g0034a0001c0002t0003g0065others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-2179_868-2176d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | ||||||
| chr8:66582541
|
CA | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0067others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.868-2176delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | ||||||
| chr8:66582648
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.868-2282C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582648 | ||||||
| chr8:66582650
|
C | T | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.868-2284G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582650 | ||||||
| chr8:66582692
|
TG | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-2327delC | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582692 | ||||||
| chr8:66582693
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-2327C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582693 | ||||||
| chr8:66582698
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-2332C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582698 | ||||||
| chr8:66582718
|
C | CA | 14 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0193others(11): Show | 14 | HG01884.hp2 HG02135.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-2353dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582718 | ||||||
| chr8:66582912
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.868-2546G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582912 | ||||||
| chr8:66583398
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.868-3032G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583398 | ||||||
| chr8:66583500
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01070.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.868-3134T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583500 | ||||||
| chr8:66583504
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0001g0157others(1): Show | 4 | HG00099.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-3138T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583504 | ||||||
| chr8:66583535
|
A | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-3169T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583535 | ||||||
| chr8:66583554
|
G | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.868-3188C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583554 | ||||||
| chr8:66583599
|
C | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.868-3233G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583599 | ||||||
| chr8:66583763
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.868-3397C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583763 | ||||||
| chr8:66584070
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.868-3704G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584070 | ||||||
| chr8:66584404
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0133others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-4038G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584404 | ||||||
| chr8:66584414
|
A | G | 1 | a0001c0001t0004g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.868-4048T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584414 | ||||||
| chr8:66584661
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.868-4295G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584661 | ||||||
| chr8:66584867
|
C | T | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.868-4501G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584867 | ||||||
| chr8:66584954
|
C | T | 3 | a0001c0001t0005g0006a0001c0001t0005g0008a0001c0001t0005g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868-4588G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584954 | ||||||
| chr8:66584976
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-4610G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584976 | ||||||
| chr8:66585088
|
AAAAC | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.868-4726_868-4723d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585088 | ||||||
| chr8:66585139
|
C | T | 1 | a0001c0001t0003g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.868-4773G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585139 | ||||||
| chr8:66585158
|
T | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.868-4792A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585158 | ||||||
| chr8:66585264
|
G | T | 5 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0061others(2): Show | 5 | HG01884.hp2 HG03225.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-4898C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585264 | ||||||
| chr8:66585356
|
T | TA | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.868-4991dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585356 | ||||||
| chr8:66585490
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.868-5124G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585490 | ||||||
| chr8:66585496
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-5130A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585496 | ||||||
| chr8:66585528
|
G | A | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868-5162C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585528 | ||||||
| chr8:66585684
|
C | T | 5 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-5318G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585684 | ||||||
| chr8:66585690
|
C | T | 1 | a0001c0001t0008g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.868-5324G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585690 | ||||||
| chr8:66585783
|
T | G | 1 | a0004c0004t0003g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.868-5417A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585783 | ||||||
| chr8:66586042
|
G | GT | 51 | a0001c0001t0001g0071a0001c0001t0001g0099a0001c0001t0001g0115others(48): Show | 55 | HG00423.hp2 HG01070.hp2 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.868-5677dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586042 | ||||||
| chr8:66586042
|
G | GTT | 10 | a0001c0001t0002g0039a0001c0001t0002g0050a0001c0001t0003g0031others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.868-5678_868-5677d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586042 | ||||||
| chr8:66586053
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.868-5687A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586053 | ||||||
| chr8:66586507
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.867+5933T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586507 | ||||||
| chr8:66586672
|
C | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00140.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.867+5768G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586672 | ||||||
| chr8:66586894
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.867+5546G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586894 | ||||||
| chr8:66586954
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.867+5486A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586954 | ||||||
| chr8:66586989
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.867+5451A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586989 | ||||||
| chr8:66587090
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0152others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+5350T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587090 | ||||||
| chr8:66587105
|
C | A | 1 | a0001c0001t0004g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.867+5335G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587105 | ||||||
| chr8:66587399
|
C | CA | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+5040dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587399 | ||||||
| chr8:66587520
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.867+4920G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587520 | ||||||
| chr8:66587691
|
G | C | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+4749C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587691 | ||||||
| chr8:66587725
|
G | A | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.867+4715C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587725 | ||||||
| chr8:66587877
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867+4563A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587877 | ||||||
| chr8:66587996
|
A | G | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+4444T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587996 | ||||||
| chr8:66588145
|
G | A | 8 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0170others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.867+4295C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588145 | ||||||
| chr8:66588277
|
C | CT | 8 | a0001c0001t0001g0021a0001c0001t0001g0163a0001c0001t0001g0199others(5): Show | 8 | HG00323.hp1 HG01071.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.867+4162dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588277 | ||||||
| chr8:66588277
|
CT | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0095others(12): Show | 15 | HG01433.hp1 HG01433.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+4162delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588277 | ||||||
| chr8:66588560
|
G | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0061others(2): Show | 5 | HG01884.hp2 HG03225.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+3880C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588560 | ||||||
| chr8:66588715
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.867+3725A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588715 | ||||||
| chr8:66588791
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0036others(7): Show | 13 | NA18946.hp1 NA18952.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.867+3649C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588791 | ||||||
| chr8:66588886
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0152 | 3 | HG02451.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.867+3554C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588886 | ||||||
| chr8:66588912
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.867+3528G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588912 | ||||||
| chr8:66589026
|
A | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.867+3414T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589026 | ||||||
| chr8:66589049
|
G | T | 1 | a0001c0001t0003g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+3391C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589049 | ||||||
| chr8:66589067
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.867+3373A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589067 | ||||||
| chr8:66589172
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+3268A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589172 | ||||||
| chr8:66589401
|
C | A | 1 | a0001c0001t0010g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.867+3039G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589401 | ||||||
| chr8:66589518
|
T | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.867+2922A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589518 | ||||||
| chr8:66589617
|
G | A | 51 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0002g0001others(48): Show | 55 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(52): Show |
intron_variant | MODIFIER | c.867+2823C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589617 | ||||||
| chr8:66589674
|
G | A | 14 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0038others(11): Show | 15 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.867+2766C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589674 | ||||||
| chr8:66589864
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.867+2576C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589864 | ||||||
| chr8:66589898
|
C | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.867+2542G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589898 | ||||||
| chr8:66590018
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.867+2422C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590018 | ||||||
| chr8:66590082
|
CCAAAA | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+2353_867+2357d others(7): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590082 | ||||||
| chr8:66590327
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.867+2113A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590327 | ||||||
| chr8:66590387
|
G | A | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+2053C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590387 | ||||||
| chr8:66590601
|
C | CA | 27 | a0001c0001t0001g0022a0001c0001t0001g0150a0001c0001t0001g0178others(24): Show | 30 | HG00438.hp2 HG02738.hp1 HG02895.hp1 others(27): Show |
intron_variant | MODIFIER | c.867+1838dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590601 | ||||||
| chr8:66591135
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.867+1305A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591135 | ||||||
| chr8:66591145
|
G | A | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(3): Show | 6 | NA18957.hp2 NA18983.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1295C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591145 | ||||||
| chr8:66591221
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+1219C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591221 | ||||||
| chr8:66591272
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.867+1168T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591272 | ||||||
| chr8:66591279
|
G | A | 23 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(20): Show | 26 | HG02523.hp2 HG02683.hp1 HG02738.hp1 others(23): Show |
intron_variant | MODIFIER | c.867+1161C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591279 | ||||||
| chr8:66591359
|
AT | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0150a0001c0001t0001g0178others(1): Show | 4 | HG00438.hp2 NA18961.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1080delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591359 | ||||||
| chr8:66591553
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.867+887T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591553 | ||||||
| chr8:66591722
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.867+718A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591722 | ||||||
| chr8:66591818
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.867+622T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591818 | ||||||
| chr8:66591861
|
A | T | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.867+579T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591861 | ||||||
| chr8:66591922
|
T | C | 3 | a0001c0001t0006g0003a0001c0001t0006g0057a0001c0001t0006g0058 | 4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+518A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591922 | ||||||
| chr8:66592097
|
C | A | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.867+343G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66592097 | ||||||
| chr8:66593206
|
T | A | 1 | a0001c0001t0014g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.688-12A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593206 | ||||||
| chr8:66593342
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.688-148G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593342 | ||||||
| chr8:66593398
|
G | A | 2 | a0001c0002t0003g0065a0001c0002t0003g0066 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.688-204C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593398 | ||||||
| chr8:66593569
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.688-375T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593569 | ||||||
| chr8:66593858
|
G | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.688-664C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593858 | ||||||
| chr8:66593885
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.688-691G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593885 | ||||||
| chr8:66593907
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.688-713C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593907 | ||||||
| chr8:66594292
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.688-1098A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594292 | ||||||
| chr8:66594437
|
A | G | 2 | a0001c0002t0003g0065a0001c0002t0003g0066 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.687+1146T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594437 | ||||||
| chr8:66594465
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.687+1118G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594465 | ||||||
| chr8:66594558
|
C | T | 21 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(18): Show | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.687+1025G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594558 | ||||||
| chr8:66595069
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.687+514A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595069 | ||||||
| chr8:66595123
|
T | C | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.687+460A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595123 | ||||||
| chr8:66595420
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.687+163T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595420 | ||||||
| chr8:66596140
|
G | A | 10 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0038others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-383C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596140 | ||||||
| chr8:66596178
|
G | A | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.513-421C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596178 | ||||||
| chr8:66596251
|
C | T | 1 | a0002c0003t0003g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.513-494G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596251 | ||||||
| chr8:66596532
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513-775A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596532 | ||||||
| chr8:66596907
|
A | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+423T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596907 | ||||||
| chr8:66596931
|
T | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.512+399A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596931 | ||||||
| chr8:66596967
|
C | T | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.512+363G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596967 | ||||||
| chr8:66597752
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.292-202T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597752 | ||||||
| chr8:66597847
|
T | TA | 39 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0019others(36): Show | 39 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-298dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | ||||||
| chr8:66597847
|
TA | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0069others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.292-298delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | ||||||
| chr8:66597847
|
TAA | T | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(25): Show | 32 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-299_292-298del others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | ||||||
| chr8:66597847
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0009g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.292-311_292-298del others(14): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | ||||||
| chr8:66598384
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.291+666G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598384 | ||||||
| chr8:66598422
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+628A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598422 | ||||||
| chr8:66598674
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.291+376A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598674 | ||||||
| chr8:66598857
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.291+193A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598857 | ||||||
| chr8:66598885
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+165G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598885 | ||||||
| chr8:66599165
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.199-23C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599165 | ||||||
| chr8:66599243
|
T | C | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.199-101A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599243 | ||||||
| chr8:66599393
|
C | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0074 | 2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.199-251G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599393 | ||||||
| chr8:66599509
|
A | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-367T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599509 | ||||||
| chr8:66599639
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-497T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599639 | ||||||
| chr8:66599731
|
T | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.199-589A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599731 | ||||||
| chr8:66599761
|
T | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-619A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599761 | ||||||
| chr8:66599850
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.199-708G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599850 | ||||||
| chr8:66599851
|
G | A | 21 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(18): Show | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.199-709C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599851 | ||||||
| chr8:66600108
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG00408.hp2 NA18992.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.199-966C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600108 | ||||||
| chr8:66600376
|
T | C | 10 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0038others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-1234A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600376 | ||||||
| chr8:66600396
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.199-1254G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600396 | ||||||
| chr8:66600644
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+1054G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600644 | ||||||
| chr8:66600660
|
C | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+1038G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600660 | ||||||
| chr8:66600760
|
T | C | 1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.198+938A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600760 | ||||||
| chr8:66600831
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.198+867C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600831 | ||||||
| chr8:66600973
|
C | T | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+725G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600973 | ||||||
| chr8:66601034
|
G | A | 10 | a0001c0001t0003g0026a0001c0001t0003g0037a0001c0001t0003g0038others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+664C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601034 | ||||||
| chr8:66601055
|
T | C | 2 | a0001c0002t0003g0065a0001c0002t0003g0066 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+643A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601055 | ||||||
| chr8:66601110
|
G | A | 5 | a0001c0001t0003g0026a0001c0001t0003g0056a0001c0001t0003g0059others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+588C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601110 | ||||||
| chr8:66601177
|
C | CA | 37 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 37 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.198+520dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601177 | ||||||
| chr8:66601177
|
CA | C | 23 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0191others(20): Show | 23 | HG01070.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+520delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601177 | ||||||
| chr8:66601362
|
T | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.198+336A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601362 | ||||||
| chr8:66601785
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.127-16T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66601785 | ||||||
| chr8:66602029
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-260T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602029 | ||||||
| chr8:66602294
|
G | A | 7 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(4): Show | 7 | NA18952.hp1 NA18957.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+124C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602294 | ||||||
| chr8:66602333
|
G | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+85C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602333 | ||||||
| chr8:66602351
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.126+67C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602351 | ||||||
| chr8:66602699
|
C | CTA | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG02738.hp2 HG04115.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-178_21-177dupTA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602699
|
C | CTATATA | 2 | a0001c0001t0001g0201a0001c0001t0013g0034 | 2 | HG02630.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.21-182_21-177dupTA others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602699
|
CTA | C | 12 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0078others(9): Show | 12 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.21-178_21-177delTA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602699
|
CTATA | C | 19 | a0001c0001t0001g0075a0001c0001t0001g0126a0001c0001t0001g0127others(16): Show | 19 | HG00099.hp2 HG00408.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.21-180_21-177delTA others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602699
|
CTATATAT others(3): Show |
C | 1 | a0002c0003t0003g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.21-186_21-177delTA others(8): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602699
|
CTATATAT others(11): Show |
C | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.21-194_21-177delTA others(16): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | ||||||
| chr8:66602713
|
ATATATAT others(16): Show |
A | 3 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG01071.hp1 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.21-213_21-191delAA others(21): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602713 | ||||||
| chr8:66602713
|
ATATATAT others(17): Show |
A | 2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | HG01070.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.21-214_21-191delAA others(22): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602713 | ||||||
| chr8:66602714
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.21-191A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602714 | ||||||
| chr8:66602717
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.21-212_21-195delAA others(16): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602717 | ||||||
| chr8:66602728
|
TA | T | 3 | a0001c0001t0001g0121a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp1 HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.21-206delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | ||||||
| chr8:66602728
|
TATA | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0221a0001c0001t0002g0044 | 3 | HG02109.hp2 HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-208_21-206delTA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | ||||||
| chr8:66602728
|
TATATA | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0003g0056others(3): Show | 6 | HG01081.hp2 HG01433.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-210_21-206delTA others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | ||||||
| chr8:66602729
|
A | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(5): Show | 8 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.21-206T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602729 | ||||||
| chr8:66602730
|
TA | T | 10 | a0001c0001t0001g0123a0001c0001t0002g0001a0001c0001t0002g0023others(7): Show | 12 | HG02895.hp1 HG02922.hp2 HG03516.hp1 others(9): Show |
intron_variant | MODIFIER | c.21-208delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602730 | ||||||
| chr8:66602730
|
TATA | T | 10 | a0001c0001t0001g0132a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 10 | HG00323.hp2 HG02135.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-210_21-208delTA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602730 | ||||||
| chr8:66602731
|
A | ATT | 3 | a0001c0001t0001g0080a0001c0001t0008g0073a0001c0001t0012g0012 | 3 | HG00140.hp1 HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.21-209_21-208insAA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | ||||||
| chr8:66602731
|
A | T | 15 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(12): Show | 15 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-208T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | ||||||
| chr8:66602731
|
ATAT | A | 9 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(6): Show | 9 | HG00423.hp1 HG02602.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-211_21-209delAT others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | ||||||
| chr8:66602731
|
ATATT | A | 10 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(7): Show | 10 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-212_21-209delAA others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | ||||||
| chr8:66602731
|
ATATTT | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0152a0001c0001t0001g0196others(3): Show | 6 | HG02523.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-213_21-209delAA others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | ||||||
| chr8:66602732
|
TA | T | 14 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0133others(11): Show | 15 | HG01074.hp1 HG01261.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-210delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602732 | ||||||
| chr8:66602733
|
A | AT | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0051others(2): Show | 5 | HG01891.hp2 NA18961.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-211dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0011g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.21-211_21-210insAA others(11): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.21-211_21-210insAA others(13): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
A | T | 54 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0077others(51): Show | 56 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.21-210T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
AT | A | 10 | a0001c0001t0001g0068a0001c0001t0001g0097a0001c0001t0001g0098others(7): Show | 10 | HG00140.hp2 HG01070.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-211delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
ATT | A | 21 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0102others(18): Show | 21 | HG00423.hp2 HG00558.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.21-212_21-211delAA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602733
|
ATTT | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0153others(7): Show | 11 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-213_21-211delAA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | ||||||
| chr8:66602734
|
T | TA | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0107others(1): Show | 4 | HG02897.hp1 HG03688.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-212_21-211insT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | ||||||
| chr8:66602734
|
T | TATATATA | 2 | a0001c0001t0010g0231a0001c0001t0010g0232 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.21-212_21-211insTA others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | ||||||
| chr8:66602734
|
T | TATATATA others(6): Show |
3 | a0001c0001t0001g0021a0001c0002t0003g0028a0004c0004t0003g0035 | 3 | HG02109.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.21-212_21-211insTA others(11): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | ||||||
| chr8:66602735
|
T | A | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(14): Show | 17 | HG00741.hp1 HG02165.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.21-212A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602735 | ||||||
| chr8:66602736
|
T | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0068others(7): Show | 10 | HG00140.hp2 HG01070.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-213A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602736 | ||||||
| chr8:66602737
|
T | A | 12 | a0001c0001t0001g0072a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG01071.hp2 HG02486.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.21-214A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602737 | ||||||
| chr8:66602738
|
T | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0110others(6): Show | 9 | HG00140.hp2 HG00323.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-215A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602738 | ||||||
| chr8:66602739
|
T | A | 3 | a0001c0001t0001g0210a0001c0002t0003g0065a0001c0002t0003g0066 | 3 | HG02486.hp2 HG03139.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.21-216A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602739 | ||||||
| chr8:66602740
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0004c0004t0003g0035 | 3 | HG02809.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-217A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602740 | ||||||
| chr8:66602741
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21-218A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602741 | ||||||
| chr8:66602742
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-219A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602742 | ||||||
| chr8:66602744
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-221A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602744 | ||||||
| chr8:66602746
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.21-223A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602746 | ||||||
| chr8:66602751
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.21-228A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602751 | ||||||
| chr8:66602761
|
T | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0056others(10): Show | 14 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-238A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602761 | ||||||
| chr8:66602847
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.21-324C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602847 | ||||||
| chr8:66602997
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.21-474C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602997 | ||||||
| chr8:66603018
|
T | A | 1 | a0001c0001t0006g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.21-495A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603018 | ||||||
| chr8:66603049
|
A | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-526T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603049 | ||||||
| chr8:66603177
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.21-654T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603177 | ||||||
| chr8:66603295
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.21-772C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603295 | ||||||
| chr8:66603310
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.21-787C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603310 | ||||||
| chr8:66603444
|
G | A | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-921C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603444 | ||||||
| chr8:66603607
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-1084G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603607 | ||||||
| chr8:66603672
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01070.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.21-1149A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603672 | ||||||
| chr8:66603706
|
G | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-1183C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603706 | ||||||
| chr8:66603747
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-1224C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603747 | ||||||
| chr8:66603812
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.21-1289G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603812 | ||||||
| chr8:66603896
|
A | G | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1373T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603896 | ||||||
| chr8:66603965
|
GA | G | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(50): Show | 57 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.21-1443delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603965 | ||||||
| chr8:66603965
|
GAA | G | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1444_21-1443del others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603965 | ||||||
| chr8:66604008
|
A | G | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1485T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604008 | ||||||
| chr8:66604052
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.21-1529A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604052 | ||||||
| chr8:66604294
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.21-1771C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604294 | ||||||
| chr8:66604551
|
T | G | 1 | a0001c0002t0003g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.21-2028A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604551 | ||||||
| chr8:66604794
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.21-2271A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604794 | ||||||
| chr8:66604979
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.21-2456A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604979 | ||||||
| chr8:66605019
|
T | C | 3 | a0001c0002t0003g0065a0001c0002t0003g0066a0004c0004t0003g0035 | 3 | HG02486.hp2 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.21-2496A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605019 | ||||||
| chr8:66605439
|
G | A | 1 | a0001c0001t0009g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.21-2916C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605439 | ||||||
| chr8:66605632
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.21-3109G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605632 | ||||||
| chr8:66605672
|
G | A | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.21-3149C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605672 | ||||||
| chr8:66605991
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.21-3468A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605991 | ||||||
| chr8:66606314
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.21-3791A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606314 | ||||||
| chr8:66606351
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(45): Show | 52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.21-3828T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606351 | ||||||
| chr8:66606593
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-4070C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606593 | ||||||
| chr8:66606712
|
T | C | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-4189A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606712 | ||||||
| chr8:66606774
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.21-4251G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606774 | ||||||
| chr8:66606786
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.21-4263C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606786 | ||||||
| chr8:66606789
|
GT | G | 7 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-4267delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606789 | ||||||
| chr8:66606936
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.21-4413C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606936 | ||||||
| chr8:66607051
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0074 | 2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.21-4528G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607051 | ||||||
| chr8:66607129
|
CA | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0208others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-4607delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607129 | ||||||
| chr8:66607131
|
A | AC | 3 | a0001c0001t0001g0014a0001c0001t0001g0206a0001c0001t0001g0221 | 3 | HG02738.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-4609_21-4608ins others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607131 | ||||||
| chr8:66607132
|
A | C | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.21-4609T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607132 | ||||||
| chr8:66607133
|
A | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0213others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-4610T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607133 | ||||||
| chr8:66607134
|
A | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0206a0001c0001t0001g0221 | 3 | HG02738.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-4611T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607134 | ||||||
| chr8:66607135
|
A | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(208): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.21-4612T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607135 | ||||||
| chr8:66607136
|
A | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0213others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-4613T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607136 | ||||||
| chr8:66607138
|
A | C | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(148): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.21-4615T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607138 | ||||||
| chr8:66607139
|
A | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0213others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.21-4616T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607139 | ||||||
| chr8:66607141
|
A | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0069others(52): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.21-4618T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607141 | ||||||
| chr8:66607144
|
A | C | 2 | a0001c0001t0001g0072a0001c0001t0008g0073 | 2 | HG02015.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.21-4621T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607144 | ||||||
| chr8:66607211
|
C | A | 2 | a0001c0002t0003g0065a0001c0002t0003g0066 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.21-4688G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607211 | ||||||
| chr8:66607470
|
C | A | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.21-4947G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607470 | ||||||
| chr8:66607518
|
C | T | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-4995G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607518 | ||||||
| chr8:66607699
|
C | CA | 62 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 66 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.20+5119dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607699 | ||||||
| chr8:66607825
|
T | C | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+4994A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607825 | ||||||
| chr8:66607837
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.20+4982G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607837 | ||||||
| chr8:66607979
|
C | A | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+4840G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607979 | ||||||
| chr8:66608107
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(34): Show | 41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.20+4712G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608107 | ||||||
| chr8:66608272
|
A | G | 11 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.20+4547T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608272 | ||||||
| chr8:66608551
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+4268C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608551 | ||||||
| chr8:66608564
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+4255T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608564 | ||||||
| chr8:66608964
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.20+3855A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608964 | ||||||
| chr8:66609124
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.20+3695A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609124 | ||||||
| chr8:66609258
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.20+3561G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609258 | ||||||
| chr8:66609376
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0015g0222 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.20+3443C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609376 | ||||||
| chr8:66609394
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20+3425T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609394 | ||||||
| chr8:66609784
|
C | T | 2 | a0002c0003t0003g0024a0002c0003t0003g0025 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+3035G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609784 | ||||||
| chr8:66610484
|
A | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02135.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.20+2335T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610484 | ||||||
| chr8:66610509
|
G | A | 2 | a0001c0002t0003g0065a0001c0002t0003g0066 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.20+2310C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610509 | ||||||
| chr8:66610522
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+2297A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610522 | ||||||
| chr8:66610547
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+2272A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610547 | ||||||
| chr8:66610595
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20+2224G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610595 | ||||||
| chr8:66610610
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20+2209T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610610 | ||||||
| chr8:66610615
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20+2204C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610615 | ||||||
| chr8:66611459
|
C | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0011g0011 | 3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+1360G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611459 | ||||||
| chr8:66611633
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.20+1186C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611633 | ||||||
| chr8:66611993
|
A | AT | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+825dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611993 | ||||||
| chr8:66612229
|
G | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(57): Show | 64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.20+590C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612229 | ||||||
| chr8:66612332
|
T | A | 1 | a0001c0001t0003g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20+487A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612332 | ||||||
| chr8:66612674
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.20+145C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612674 | ||||||
| chr8:66612714
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20+105C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612714 | ||||||
| chr8:66612737
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.20+82C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612737 | ||||||
| chr8:66612777
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20+42C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612777 |