Search by Gene
| geneid | 57708 |
|---|---|
| ensemblid | ENSG00000198160.15 |
| hgncid | 29657 |
| symbol | MIER1 |
| name | MIER1 transcriptional regulator |
| refseq_nuc | NM_001077700.3 |
| refseq_prot | NP_001071168.2 |
| ensembl_nuc | ENST00000401041.6 |
| ensembl_prot | ENSP00000383820.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 66924990 |
| end | 66988619 |
| strand | + |
| ver | v1.2 |
| region | chr1:66924990-66988619 |
| region5000 | chr1:66919990-66993619 |
| regionname0 | MIER1_chr1_66924990_66988619 |
| regionname5000 | MIER1_chr1_66919990_66993619 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 565 | 245 | 84 | 39 | 80 | 12 | 28 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0002 | 0/0 | 565 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0003 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1698 | 240 | 79 | 39 | 80 | 12 | 28 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| c0002 | 0/0 | 1698 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| c0003 | 0/0 | 1698 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| c0004 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| c0005 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| c0006 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3759 | 68 | 13 | 4 | 38 | 2 | 10 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0002 | 0/0 | 3773 | 24 | 8 | 3 | 7 | 2 | 4 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0003 | 0/0 | 3772 | 22 | 0 | 5 | 13 | 2 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0004 | 0/0 | 3754 | 21 | 17 | 4 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0005 | 0/0 | 3759 | 17 | 9 | 2 | 3 | 1 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0006 | 0/0 | 3758 | 13 | 2 | 5 | 6 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0007 | 0/0 | 3758 | 11 | 1 | 5 | 1 | 2 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0008 | 0/0 | 3758 | 9 | 9 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0009 | 1/0 | 3759 | 8 | 0 | 4 | 0 | 1 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0010 | 0/0 | 3753 | 5 | 4 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0011 | 0/0 | 3760 | 5 | 0 | 3 | 0 | 0 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0012 | 0/0 | 3758 | 4 | 2 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0013 | 0/0 | 3774 | 4 | 2 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0014 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0015 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0016 | 0/0 | 3759 | 3 | 0 | 0 | 0 | 0 | 3 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0017 | 0/0 | 3761 | 3 | 2 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0018 | 0/0 | 3776 | 3 | 0 | 0 | 3 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0019 | 0/0 | 3757 | 2 | 0 | 0 | 1 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0020 | 0/0 | 3774 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0021 | 0/0 | 3758 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0022 | 0/0 | 3759 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0023 | 0/0 | 3759 | 2 | 0 | 1 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0024 | 0/0 | 3755 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0025 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0026 | 0/0 | 3773 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0027 | 0/0 | 3772 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0028 | 0/0 | 3773 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0029 | 0/0 | 3774 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0030 | 0/0 | 3774 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0031 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0032 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0033 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0034 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| t0035 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0193 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 240 | 79 | 39 | 80 | 12 | 28 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 65 | 11 | 3 | 38 | 2 | 10 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 24 | 8 | 3 | 7 | 2 | 4 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 22 | 0 | 5 | 13 | 2 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 20 | 17 | 3 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 17 | 9 | 2 | 3 | 1 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 12 | 2 | 4 | 6 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 11 | 1 | 5 | 1 | 2 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 1/0 | 8 | 0 | 4 | 0 | 1 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| a0003c0006t0004 | a0003 | c0006 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0014 | a0001 | c0001 | t0002 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0180 | a0001 | c0001 | t0002 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0182 | a0001 | c0001 | t0002 | g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0183 | a0001 | c0001 | t0002 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0184 | a0001 | c0001 | t0002 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0200 | a0001 | c0001 | t0002 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0201 | a0001 | c0001 | t0002 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0213 | a0001 | c0001 | t0002 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0179 | a0001 | c0001 | t0003 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0188 | a0001 | c0001 | t0003 | g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0191 | a0001 | c0001 | t0003 | g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0202 | a0001 | c0001 | t0003 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0204 | a0001 | c0001 | t0003 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0205 | a0001 | c0001 | t0003 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0206 | a0001 | c0001 | t0003 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0207 | a0001 | c0001 | t0003 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0208 | a0001 | c0001 | t0003 | g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0210 | a0001 | c0001 | t0003 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0211 | a0001 | c0001 | t0003 | g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0216 | a0001 | c0001 | t0003 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0217 | a0001 | c0001 | t0003 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0218 | a0001 | c0001 | t0003 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0219 | a0001 | c0001 | t0003 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0221 | a0001 | c0001 | t0003 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0222 | a0001 | c0001 | t0003 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0223 | a0001 | c0001 | t0003 | g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0224 | a0001 | c0001 | t0003 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0003g0227 | a0001 | c0001 | t0003 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0004 | a0001 | c0001 | t0004 | g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0008 | a0001 | c0001 | t0004 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0015 | a0001 | c0001 | t0004 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0016 | a0001 | c0001 | t0004 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0019 | a0001 | c0001 | t0004 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0020 | a0001 | c0001 | t0004 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0021 | a0001 | c0001 | t0004 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0023 | a0001 | c0001 | t0004 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0026 | a0001 | c0001 | t0004 | g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0027 | a0001 | c0001 | t0004 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0028 | a0001 | c0001 | t0004 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0029 | a0001 | c0001 | t0004 | g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0053 | a0001 | c0001 | t0004 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0054 | a0001 | c0001 | t0004 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0055 | a0001 | c0001 | t0004 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0056 | a0001 | c0001 | t0004 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0058 | a0001 | c0001 | t0004 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0004g0059 | a0001 | c0001 | t0004 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0005 | a0001 | c0001 | t0005 | g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0006 | a0001 | c0001 | t0005 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0030 | a0001 | c0001 | t0005 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0031 | a0001 | c0001 | t0005 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0032 | a0001 | c0001 | t0005 | g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0033 | a0001 | c0001 | t0005 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0034 | a0001 | c0001 | t0005 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0037 | a0001 | c0001 | t0005 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0039 | a0001 | c0001 | t0005 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0041 | a0001 | c0001 | t0005 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0042 | a0001 | c0001 | t0005 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0043 | a0001 | c0001 | t0005 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0044 | a0001 | c0001 | t0005 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0045 | a0001 | c0001 | t0005 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0046 | a0001 | c0001 | t0005 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0005g0047 | a0001 | c0001 | t0005 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0001 | a0001 | c0001 | t0006 | g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0010 | a0001 | c0001 | t0006 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0096 | a0001 | c0001 | t0006 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0113 | a0001 | c0001 | t0006 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0114 | a0001 | c0001 | t0006 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0115 | a0001 | c0001 | t0006 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0127 | a0001 | c0001 | t0006 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0130 | a0001 | c0001 | t0006 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0132 | a0001 | c0001 | t0006 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0006g0135 | a0001 | c0001 | t0006 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0060 | a0001 | c0001 | t0007 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0063 | a0001 | c0001 | t0007 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0064 | a0001 | c0001 | t0007 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0065 | a0001 | c0001 | t0007 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0076 | a0001 | c0001 | t0007 | g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0077 | a0001 | c0001 | t0007 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0078 | a0001 | c0001 | t0007 | g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0079 | a0001 | c0001 | t0007 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0080 | a0001 | c0001 | t0007 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0081 | a0001 | c0001 | t0007 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0007g0083 | a0001 | c0001 | t0007 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0009 | a0001 | c0001 | t0008 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0051 | a0001 | c0001 | t0008 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0052 | a0001 | c0001 | t0008 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0071 | a0001 | c0001 | t0008 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0072 | a0001 | c0001 | t0008 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0073 | a0001 | c0001 | t0008 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0074 | a0001 | c0001 | t0008 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0008g0075 | a0001 | c0001 | t0008 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0009g0003 | a0001 | c0001 | t0009 | g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0009g0012 | a0001 | c0001 | t0009 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0009g0129 | a0001 | c0001 | t0009 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0009g0143 | a0001 | c0001 | t0009 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0009g0193 | a0001 | c0001 | t0009 | g0193 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0010g0008 | a0001 | c0001 | t0010 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0010g0018 | a0001 | c0001 | t0010 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0010g0025 | a0001 | c0001 | t0010 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0010g0066 | a0001 | c0001 | t0010 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0010g0067 | a0001 | c0001 | t0010 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0011g0104 | a0001 | c0001 | t0011 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0011g0141 | a0001 | c0001 | t0011 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0011g0145 | a0001 | c0001 | t0011 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0011g0155 | a0001 | c0001 | t0011 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0011g0162 | a0001 | c0001 | t0011 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0012g0006 | a0001 | c0001 | t0012 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0012g0024 | a0001 | c0001 | t0012 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0012g0035 | a0001 | c0001 | t0012 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0012g0036 | a0001 | c0001 | t0012 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0013g0172 | a0001 | c0001 | t0013 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0013g0173 | a0001 | c0001 | t0013 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0013g0176 | a0001 | c0001 | t0013 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0013g0177 | a0001 | c0001 | t0013 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0014g0007 | a0001 | c0001 | t0014 | g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0014g0040 | a0001 | c0001 | t0014 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0016g0084 | a0001 | c0001 | t0016 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0016g0090 | a0001 | c0001 | t0016 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0016g0092 | a0001 | c0001 | t0016 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0017g0061 | a0001 | c0001 | t0017 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0017g0062 | a0001 | c0001 | t0017 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0017g0082 | a0001 | c0001 | t0017 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0018g0185 | a0001 | c0001 | t0018 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0018g0209 | a0001 | c0001 | t0018 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0018g0228 | a0001 | c0001 | t0018 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0019g0002 | a0001 | c0001 | t0019 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0019g0093 | a0001 | c0001 | t0019 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0020g0225 | a0001 | c0001 | t0020 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0020g0226 | a0001 | c0001 | t0020 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0021g0068 | a0001 | c0001 | t0021 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0021g0070 | a0001 | c0001 | t0021 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0022g0100 | a0001 | c0001 | t0022 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0022g0101 | a0001 | c0001 | t0022 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0023g0102 | a0001 | c0001 | t0023 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0023g0105 | a0001 | c0001 | t0023 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0024g0017 | a0001 | c0001 | t0024 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0025g0038 | a0001 | c0001 | t0025 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0026g0171 | a0001 | c0001 | t0026 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0027g0220 | a0001 | c0001 | t0027 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0028g0181 | a0001 | c0001 | t0028 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0029g0178 | a0001 | c0001 | t0029 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0030g0174 | a0001 | c0001 | t0030 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0031g0069 | a0001 | c0001 | t0031 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0032g0146 | a0001 | c0001 | t0032 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0033g0150 | a0001 | c0001 | t0033 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0034g0138 | a0001 | c0001 | t0034 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0001t0035g0175 | a0001 | c0001 | t0035 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0002t0015g0048 | a0001 | c0002 | t0015 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0002t0015g0049 | a0001 | c0002 | t0015 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0002t0015g0050 | a0001 | c0002 | t0015 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0004t0001g0095 | a0001 | c0004 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0001c0005t0001g0125 | a0001 | c0005 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0002c0003t0001g0119 | a0002 | c0003 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0002c0003t0006g0137 | a0002 | c0003 | t0006 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| a0003c0006t0004g0057 | a0003 | c0006 | t0004 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0019 | g0093 | EUR | GBR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0065 | EUR | GBR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00621 | hp2 | a0001 | c0001 | t0032 | g0146 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0066 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00639 | hp2 | a0001 | c0001 | t0028 | g0181 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00738 | hp1 | a0003 | c0006 | t0004 | g0057 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0119 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0129 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0079 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0114 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0081 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01109 | hp2 | a0001 | c0001 | t0033 | g0150 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0172 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0173 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01192 | hp2 | a0001 | c0001 | t0026 | g0171 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01256 | hp1 | a0001 | c0001 | t0023 | g0105 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01256 | hp2 | a0002 | c0003 | t0006 | g0137 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0003 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0211 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01517 | hp2 | a0001 | c0001 | t0023 | g0102 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01934 | hp2 | a0001 | c0001 | t0011 | g0145 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02132 | hp1 | a0001 | c0001 | t0027 | g0220 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | CDX | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0226 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0070 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0176 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0155 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0162 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0125 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02523 | hp1 | a0001 | c0001 | t0017 | g0082 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02523 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0095 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0143 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0075 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0061 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02630 | hp2 | a0001 | c0001 | t0035 | g0175 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0225 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02738 | hp2 | a0001 | c0001 | t0016 | g0090 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02818 | hp2 | a0001 | c0002 | t0015 | g0049 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0040 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0067 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02970 | hp1 | a0001 | c0001 | t0030 | g0174 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0024 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0006 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03209 | hp1 | a0001 | c0002 | t0015 | g0050 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03225 | hp2 | a0001 | c0001 | t0031 | g0069 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0076 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0141 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03491 | hp2 | a0001 | c0001 | t0016 | g0092 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03516 | hp1 | a0001 | c0001 | t0029 | g0178 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03654 | hp2 | a0001 | c0001 | t0025 | g0038 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03669 | hp1 | a0001 | c0001 | t0016 | g0084 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0044 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0080 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0104 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0039 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18960 | hp1 | a0001 | c0001 | t0022 | g0100 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18979 | hp1 | a0001 | c0001 | t0022 | g0101 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18980 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0035 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18986 | hp2 | a0001 | c0001 | t0018 | g0185 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19003 | hp2 | a0001 | c0001 | t0018 | g0209 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19058 | hp1 | a0001 | c0001 | t0018 | g0228 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19079 | hp1 | a0001 | c0001 | t0034 | g0138 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | ASW | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0048 | AFR | ASW | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0046 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0060 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | GIH | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02109 | hp2 | a0001 | c0001 | t0021 | g0068 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG02559 | hp2 | a0001 | c0001 | t0024 | g0017 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0071 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0177 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | MIER1_chr1_66919990_66993619 | MIER1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0193 | REF | REF | MIER1_chr1_66919990_66993619 | MIER1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66958089
|
A | T | 1 | a0003 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.370A>T | p.Ser124Cys | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/14 | 409/5456 | 370/1698 | 124/565 | chr1 | 66958089 | ||
| chr1:66984748
|
A | G | 1 | a0002 | 2 | HG00738.hp2 HG01256.hp2 |
missense_variant | MODERATE | c.1546A>G | p.Arg516Gly | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1585/5456 | 1546/1698 | 516/565 | chr1 | 66984748 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66926188
|
G | A | 1 | a0001c0004 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.114G>A | p.Thr38Thr | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/14 | 153/5456 | 114/1698 | 38/565 | chr1 | 66926188 | ||
| chr1:66970935
|
A | C | 1 | a0001c0002 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.900A>C | p.Gly300Gly | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/14 | 939/5456 | 900/1698 | 300/565 | chr1 | 66970935 | ||
| chr1:66984612
|
G | A | 1 | a0001c0005 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1410G>A | p.Glu470Glu | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1449/5456 | 1410/1698 | 470/565 | chr1 | 66984612 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66985804
|
G | A | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(5): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 904 | chr1 | 66985804 | |||||
| chr1:66985814
|
A | AT | 1 | a0001c0001t0011 | 5 | HG01934.hp2 HG02293.hp1 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 938 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | ||||
| chr1:66985814
|
AT | A | 5 | a0001c0001t0006a0001c0001t0021a0001c0001t0025others(2): Show | 17 | HG00423.hp1 HG01106.hp1 HG01256.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*937delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 937 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | ||||
| chr1:66985814
|
ATT | A | 7 | a0001c0001t0005a0001c0001t0014a0001c0001t0019others(4): Show | 27 | HG00140.hp1 HG01106.hp2 HG01255.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*937delTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 936 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | ||||
| chr1:66985814
|
ATTT | A | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(5): Show | 66 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*935_*937delTTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 935 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | ||||
| chr1:66985814
|
ATTTT | A | 4 | a0001c0001t0003a0001c0001t0010a0001c0001t0026others(1): Show | 29 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*934_*937delTTTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 934 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | ||||
| chr1:66985835
|
TTTA | T | 1 | a0001c0001t0007 | 11 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*938delTTA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 936 | chr1 | 66985835 | |||||
| chr1:66985919
|
A | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(8): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1019A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1019 | chr1 | 66985919 | |||||
| chr1:66986047
|
T | C | 1 | a0001c0001t0032 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1147 | chr1 | 66986047 | |||||
| chr1:66986215
|
A | G | 1 | a0001c0001t0014 | 3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1315 | chr1 | 66986215 | |||||
| chr1:66986239
|
C | T | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(7): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1339C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1339 | chr1 | 66986239 | |||||
| chr1:66986241
|
G | T | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(7): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1341G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1341 | chr1 | 66986241 | |||||
| chr1:66986254
|
T | C | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1354 | chr1 | 66986254 | |||||
| chr1:66986457
|
A | G | 1 | a0001c0001t0034 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1557A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1557 | chr1 | 66986457 | |||||
| chr1:66986639
|
G | A | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(7): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1739G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1739 | chr1 | 66986639 | |||||
| chr1:66986731
|
G | T | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(5): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1831G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1831 | chr1 | 66986731 | |||||
| chr1:66986799
|
G | A | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(5): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1899 | chr1 | 66986799 | |||||
| chr1:66986864
|
G | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1964 | chr1 | 66986864 | |||||
| chr1:66986866
|
A | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1966A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1966 | chr1 | 66986866 | |||||
| chr1:66986868
|
C | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1968 | chr1 | 66986868 | |||||
| chr1:66986869
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1969 | chr1 | 66986869 | |||||
| chr1:66986870
|
T | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1970 | chr1 | 66986870 | |||||
| chr1:66986872
|
G | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1972G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1972 | chr1 | 66986872 | |||||
| chr1:66986875
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1975 | chr1 | 66986875 | |||||
| chr1:66986879
|
G | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1979G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1979 | chr1 | 66986879 | |||||
| chr1:66986880
|
T | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1980 | chr1 | 66986880 | |||||
| chr1:66986890
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1990 | chr1 | 66986890 | |||||
| chr1:66986893
|
G | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1993 | chr1 | 66986893 | |||||
| chr1:66986894
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1994 | chr1 | 66986894 | |||||
| chr1:66986898
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1998A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1998 | chr1 | 66986898 | |||||
| chr1:66986903
|
T | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2003 | chr1 | 66986903 | |||||
| chr1:66986904
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2004T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2004 | chr1 | 66986904 | |||||
| chr1:66986905
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2005 | chr1 | 66986905 | |||||
| chr1:66986909
|
A | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2009 | chr1 | 66986909 | |||||
| chr1:66986916
|
G | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2016G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2016 | chr1 | 66986916 | |||||
| chr1:66986918
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2018 | chr1 | 66986918 | |||||
| chr1:66986924
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2024T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2024 | chr1 | 66986924 | |||||
| chr1:66986925
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2025A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2025 | chr1 | 66986925 | |||||
| chr1:66986935
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2035 | chr1 | 66986935 | |||||
| chr1:66986936
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2036 | chr1 | 66986936 | |||||
| chr1:66986938
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2038T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2038 | chr1 | 66986938 | |||||
| chr1:66986939
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2039T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2039 | chr1 | 66986939 | |||||
| chr1:66986940
|
G | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2040 | chr1 | 66986940 | |||||
| chr1:66986945
|
G | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2045G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2045 | chr1 | 66986945 | |||||
| chr1:66986951
|
G | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2051 | chr1 | 66986951 | |||||
| chr1:66986952
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2052 | chr1 | 66986952 | |||||
| chr1:66986953
|
T | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2053T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2053 | chr1 | 66986953 | |||||
| chr1:66986955
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2055C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2055 | chr1 | 66986955 | |||||
| chr1:66986956
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2056C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2056 | chr1 | 66986956 | |||||
| chr1:66986960
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2060T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2060 | chr1 | 66986960 | |||||
| chr1:66986961
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2061T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2061 | chr1 | 66986961 | |||||
| chr1:66986963
|
A | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2063A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2063 | chr1 | 66986963 | |||||
| chr1:66986964
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2064C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2064 | chr1 | 66986964 | |||||
| chr1:66986965
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2065 | chr1 | 66986965 | |||||
| chr1:66986974
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2074A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2074 | chr1 | 66986974 | |||||
| chr1:66986975
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2075A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2075 | chr1 | 66986975 | |||||
| chr1:66986976
|
G | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2076G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2076 | chr1 | 66986976 | |||||
| chr1:66986981
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2081A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2081 | chr1 | 66986981 | |||||
| chr1:66986982
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2082 | chr1 | 66986982 | |||||
| chr1:66986984
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2084 | chr1 | 66986984 | |||||
| chr1:66986985
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2085T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2085 | chr1 | 66986985 | |||||
| chr1:66986986
|
A | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2086 | chr1 | 66986986 | |||||
| chr1:66986988
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2088 | chr1 | 66986988 | |||||
| chr1:66986991
|
C | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2091C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2091 | chr1 | 66986991 | |||||
| chr1:66986992
|
A | T | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2092A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2092 | chr1 | 66986992 | |||||
| chr1:66986996
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2096 | chr1 | 66986996 | |||||
| chr1:66987001
|
A | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2101A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2101 | chr1 | 66987001 | |||||
| chr1:66987004
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2104 | chr1 | 66987004 | |||||
| chr1:66987008
|
T | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2108T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2108 | chr1 | 66987008 | |||||
| chr1:66987009
|
G | C | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2109 | chr1 | 66987009 | |||||
| chr1:66987011
|
A | G | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2111 | chr1 | 66987011 | |||||
| chr1:66987023
|
C | T | 1 | a0001c0001t0033 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2123 | chr1 | 66987023 | |||||
| chr1:66987034
|
T | A | 1 | a0001c0001t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2134T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2134 | chr1 | 66987034 | |||||
| chr1:66987037
|
A | G | 1 | a0001c0001t0027 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2137A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2137 | chr1 | 66987037 | |||||
| chr1:66987146
|
T | A | 1 | a0001c0001t0021 | 2 | HG02109.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2246T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2246 | chr1 | 66987146 | |||||
| chr1:66987352
|
A | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*2452A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2452 | chr1 | 66987352 | |||||
| chr1:66987417
|
C | A | 1 | a0001c0001t0020 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2517 | chr1 | 66987417 | |||||
| chr1:66987437
|
A | AT | 3 | a0001c0001t0013a0001c0001t0026a0001c0001t0035 | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2541dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2542 | INFO_REALIGN_3_PRIME | chr1 | 66987437 | ||||
| chr1:66987762
|
A | AAT | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(4): Show | 48 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2874_*2875dupTA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2876 | INFO_REALIGN_3_PRIME | chr1 | 66987762 | ||||
| chr1:66987907
|
G | C | 1 | a0001c0001t0020 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3007G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3007 | chr1 | 66987907 | |||||
| chr1:66987918
|
ACT | A | 4 | a0001c0001t0004a0001c0001t0010a0001c0001t0024others(1): Show | 27 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3021_*3022delCT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3021 | INFO_REALIGN_3_PRIME | chr1 | 66987918 | ||||
| chr1:66987947
|
A | C | 1 | a0001c0001t0023 | 2 | HG01256.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3047A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3047 | chr1 | 66987947 | |||||
| chr1:66987968
|
G | A | 1 | a0001c0001t0016 | 3 | HG02738.hp2 HG03491.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3068G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3068 | chr1 | 66987968 | |||||
| chr1:66988113
|
T | TGTGTGCT others(10): Show |
11 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(8): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3214_*3215insTGTG others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3215 | INFO_REALIGN_3_PRIME | chr1 | 66988113 | ||||
| chr1:66988408
|
A | T | 1 | a0001c0001t0020 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3508A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3508 | chr1 | 66988408 | |||||
| chr1:66988450
|
A | G | 1 | a0001c0001t0022 | 2 | NA18960.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3550A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3550 | chr1 | 66988450 | |||||
| chr1:66988513
|
C | T | 1 | a0001c0002t0015 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3613C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3613 | chr1 | 66988513 | |||||
| chr1:66988554
|
A | G | 2 | a0001c0001t0021a0001c0001t0031 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3654A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3654 | chr1 | 66988554 | |||||
| chr1:66988604
|
A | G | 3 | a0001c0001t0007a0001c0001t0008a0001c0001t0017 | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3704A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3704 | chr1 | 66988604 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66925175
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.67+80C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925175 | ||||||
| chr1:66925316
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.67+221G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925316 | ||||||
| chr1:66925320
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.67+225G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925320 | ||||||
| chr1:66925324
|
C | T | 2 | a0001c0001t0003g0227a0001c0001t0018g0228 | 2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.67+229C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925324 | ||||||
| chr1:66925520
|
A | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.67+425A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925520 | ||||||
| chr1:66925642
|
G | C | 16 | a0001c0001t0004g0004a0001c0001t0004g0015a0001c0001t0004g0016others(13): Show | 17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-500G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925642 | ||||||
| chr1:66926813
|
T | C | 3 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0026g0171 | 3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.168+571T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926813 | ||||||
| chr1:66926931
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.168+689A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926931 | ||||||
| chr1:66926963
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.168+721A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926963 | ||||||
| chr1:66927031
|
A | G | 11 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218others(8): Show | 11 | HG00423.hp2 HG01243.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+789A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927031 | ||||||
| chr1:66927206
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.168+964G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927206 | ||||||
| chr1:66927730
|
G | T | 2 | a0001c0001t0007g0083a0001c0001t0017g0082 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.168+1488G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927730 | ||||||
| chr1:66928145
|
G | A | 11 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(8): Show | 11 | HG00140.hp1 HG02080.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1903G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928145 | ||||||
| chr1:66928217
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+1975A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928217 | ||||||
| chr1:66928960
|
C | T | 1 | a0001c0001t0007g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+2718C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928960 | ||||||
| chr1:66929024
|
AG | A | 22 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0030others(19): Show | 24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+2783delG | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929024 | ||||||
| chr1:66929235
|
A | G | 5 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0079others(2): Show | 5 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+2993A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929235 | ||||||
| chr1:66929548
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0006g0010a0001c0001t0006g0096others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+3306T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929548 | ||||||
| chr1:66929636
|
G | A | 1 | a0001c0001t0004g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.168+3394G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929636 | ||||||
| chr1:66929652
|
A | C | 16 | a0001c0001t0004g0004a0001c0001t0004g0015a0001c0001t0004g0016others(13): Show | 17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+3410A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929652 | ||||||
| chr1:66929960
|
G | A | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+3718G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929960 | ||||||
| chr1:66930224
|
G | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02027.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.168+3982G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930224 | ||||||
| chr1:66930539
|
T | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(181): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.168+4297T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930539 | ||||||
| chr1:66930544
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.168+4302G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930544 | ||||||
| chr1:66930748
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.168+4506C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930748 | ||||||
| chr1:66930811
|
C | T | 3 | a0001c0001t0005g0045a0001c0001t0005g0046a0001c0001t0005g0047 | 3 | HG01106.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.168+4569C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930811 | ||||||
| chr1:66930876
|
C | G | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+4634C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930876 | ||||||
| chr1:66931010
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168+4768C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931010 | ||||||
| chr1:66931056
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.168+4814C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931056 | ||||||
| chr1:66931069
|
C | A | 6 | a0001c0001t0005g0005a0001c0001t0005g0030a0001c0001t0005g0031others(3): Show | 7 | HG01255.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+4827C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931069 | ||||||
| chr1:66931221
|
G | T | 4 | a0001c0001t0002g0014a0001c0001t0002g0213a0001c0001t0002g0214others(1): Show | 5 | NA18954.hp1 NA18965.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4979G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931221 | ||||||
| chr1:66931491
|
T | G | 1 | a0001c0001t0016g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+5249T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931491 | ||||||
| chr1:66931525
|
G | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.168+5283G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931525 | ||||||
| chr1:66931593
|
A | G | 5 | a0001c0001t0008g0009a0001c0001t0008g0072a0001c0001t0008g0073others(2): Show | 6 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+5351A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931593 | ||||||
| chr1:66931597
|
C | A | 1 | a0001c0001t0004g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.168+5355C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931597 | ||||||
| chr1:66931641
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168+5399C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931641 | ||||||
| chr1:66931728
|
G | A | 2 | a0001c0001t0008g0051a0001c0001t0008g0052 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168+5486G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931728 | ||||||
| chr1:66931970
|
G | A | 2 | a0001c0001t0012g0035a0001c0001t0012g0036 | 2 | NA18980.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.168+5728G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931970 | ||||||
| chr1:66931974
|
T | C | 1 | a0001c0001t0030g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+5732T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931974 | ||||||
| chr1:66932182
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.168+5940T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932182 | ||||||
| chr1:66932340
|
T | A | 1 | a0001c0001t0003g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+6098T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932340 | ||||||
| chr1:66932435
|
G | C | 25 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(22): Show | 26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.168+6193G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932435 | ||||||
| chr1:66932436
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.168+6194A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932436 | ||||||
| chr1:66932501
|
T | A | 2 | a0001c0001t0022g0100a0001c0001t0022g0101 | 2 | NA18960.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.168+6259T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932501 | ||||||
| chr1:66932751
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168+6509C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932751 | ||||||
| chr1:66932816
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+6574A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932816 | ||||||
| chr1:66932870
|
A | G | 1 | a0001c0001t0009g0012 | 2 | HG01099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.168+6628A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932870 | ||||||
| chr1:66932924
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.168+6682G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932924 | ||||||
| chr1:66932950
|
A | G | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+6708A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932950 | ||||||
| chr1:66933035
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0006g0010a0001c0001t0006g0096others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+6793C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933035 | ||||||
| chr1:66933233
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.169-6795G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933233 | ||||||
| chr1:66933355
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.169-6673A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933355 | ||||||
| chr1:66933364
|
T | C | 2 | a0001c0001t0006g0096a0001c0004t0001g0095 | 2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.169-6664T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933364 | ||||||
| chr1:66933754
|
A | G | 8 | a0001c0001t0008g0009a0001c0001t0008g0051a0001c0001t0008g0052others(5): Show | 9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-6274A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933754 | ||||||
| chr1:66933783
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(181): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.169-6245T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933783 | ||||||
| chr1:66934143
|
A | G | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5885A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934143 | ||||||
| chr1:66934247
|
A | G | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5781A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934247 | ||||||
| chr1:66934391
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.169-5637C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934391 | ||||||
| chr1:66934405
|
C | CT | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(142): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.169-5607dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934405 | |||||
| chr1:66934405
|
C | CTT | 9 | a0001c0001t0001g0164a0001c0001t0013g0172a0001c0001t0013g0173others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-5608_169-5607d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934405 | |||||
| chr1:66934414
|
T | C | 1 | a0001c0001t0002g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-5614T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934414 | ||||||
| chr1:66934472
|
A | G | 1 | a0001c0001t0020g0226 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-5556A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934472 | ||||||
| chr1:66934572
|
C | CT | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.169-5442dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934572 | |||||
| chr1:66934572
|
C | CTT | 5 | a0001c0001t0001g0163a0001c0001t0004g0028a0001c0001t0004g0029others(2): Show | 5 | HG01192.hp1 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-5443_169-5442d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934572 | |||||
| chr1:66934626
|
G | A | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169-5402G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934626 | ||||||
| chr1:66934844
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.169-5184G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934844 | ||||||
| chr1:66935118
|
A | T | 27 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.169-4910A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935118 | ||||||
| chr1:66935448
|
C | T | 1 | a0001c0001t0011g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.169-4580C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935448 | ||||||
| chr1:66935552
|
T | G | 1 | a0001c0001t0007g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.169-4476T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935552 | ||||||
| chr1:66935899
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.169-4129A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935899 | ||||||
| chr1:66935940
|
ACT | A | 14 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(11): Show | 14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4087_169-4086d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935940 | ||||||
| chr1:66935943
|
T | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-4085T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935943 | ||||||
| chr1:66935946
|
A | G | 14 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(11): Show | 14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4082A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935946 | ||||||
| chr1:66935947
|
A | C | 14 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(11): Show | 14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4081A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935947 | ||||||
| chr1:66935979
|
T | C | 1 | a0001c0001t0023g0105 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.169-4049T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935979 | ||||||
| chr1:66936278
|
G | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.169-3750G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936278 | ||||||
| chr1:66936283
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0003g0210 | 2 | NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.169-3745C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936283 | ||||||
| chr1:66936722
|
C | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.169-3306C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936722 | ||||||
| chr1:66936771
|
C | T | 1 | a0001c0001t0029g0178 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.169-3257C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936771 | ||||||
| chr1:66936913
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.169-3115T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936913 | ||||||
| chr1:66936985
|
C | T | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3043C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936985 | ||||||
| chr1:66936998
|
C | CA | 7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG00558.hp1 HG00639.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-3008dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | |||||
| chr1:66936998
|
CA | C | 93 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0085others(90): Show | 97 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.169-3008delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | |||||
| chr1:66936998
|
CAA | C | 36 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0003g0013others(33): Show | 37 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.169-3009_169-3008d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | |||||
| chr1:66936998
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.169-3020_169-3008d others(15): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | |||||
| chr1:66937021
|
G | A | 1 | a0001c0001t0021g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169-3007G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937021 | ||||||
| chr1:66937023
|
G | A | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3005G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937023 | ||||||
| chr1:66937149
|
C | T | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.169-2879C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937149 | ||||||
| chr1:66937155
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(175): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.169-2873T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937155 | ||||||
| chr1:66937156
|
G | A | 1 | a0001c0001t0018g0185 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.169-2872G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937156 | ||||||
| chr1:66937270
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.169-2758G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937270 | ||||||
| chr1:66937335
|
C | G | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-2693C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937335 | ||||||
| chr1:66937588
|
AAAAAG | A | 27 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.169-2425_169-2421d others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66937588 | |||||
| chr1:66937632
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.169-2396C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937632 | ||||||
| chr1:66938104
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.169-1924G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938104 | ||||||
| chr1:66938235
|
A | G | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.169-1793A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938235 | ||||||
| chr1:66938290
|
A | G | 2 | a0001c0001t0007g0064a0001c0001t0007g0065 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.169-1738A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938290 | ||||||
| chr1:66938817
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169-1211A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938817 | ||||||
| chr1:66938836
|
T | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0161 | 3 | HG00621.hp1 NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.169-1192T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938836 | ||||||
| chr1:66939195
|
A | G | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.169-833A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939195 | ||||||
| chr1:66939227
|
T | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(175): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.169-801T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939227 | ||||||
| chr1:66939367
|
G | A | 25 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(22): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.169-661G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939367 | ||||||
| chr1:66939374
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(173): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.169-654G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939374 | ||||||
| chr1:66939509
|
A | G | 3 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0026g0171 | 3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.169-519A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939509 | ||||||
| chr1:66939781
|
C | G | 1 | a0001c0001t0030g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.169-247C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939781 | ||||||
| chr1:66939919
|
A | G | 1 | a0002c0003t0006g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.169-109A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939919 | ||||||
| chr1:66939963
|
C | T | 2 | a0001c0001t0021g0068a0001c0001t0021g0070 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.169-65C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939963 | ||||||
| chr1:66940270
|
CT | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(152): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.193+239delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66940270 | |||||
| chr1:66940270
|
CTT | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0002g0212others(2): Show | 5 | HG02976.hp2 NA18954.hp2 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+238_193+239del others(2): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66940270 | |||||
| chr1:66940273
|
T | TC | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+221_193+222ins others(1): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940273 | ||||||
| chr1:66940462
|
G | A | 3 | a0001c0001t0004g0008a0001c0001t0004g0053a0001c0001t0010g0008 | 3 | HG02630.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193+410G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940462 | ||||||
| chr1:66940482
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.193+430C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940482 | ||||||
| chr1:66940854
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.193+802G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940854 | ||||||
| chr1:66940908
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193+856G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940908 | ||||||
| chr1:66941279
|
G | A | 27 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.193+1227G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941279 | ||||||
| chr1:66941323
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193+1271C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941323 | ||||||
| chr1:66941451
|
T | G | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+1399T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941451 | ||||||
| chr1:66941550
|
C | T | 1 | a0001c0001t0011g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+1498C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941550 | ||||||
| chr1:66941821
|
A | G | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.193+1769A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941821 | ||||||
| chr1:66941863
|
G | A | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193+1811G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941863 | ||||||
| chr1:66941970
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(140): Show | 154 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.193+1935dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | |||||
| chr1:66941970
|
C | CAA | 13 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0004g0008others(10): Show | 13 | HG02074.hp2 HG02257.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+1934_193+1935d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | |||||
| chr1:66941970
|
C | CAAA | 13 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 13 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.193+1933_193+1935d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | |||||
| chr1:66941970
|
C | CAAAA | 5 | a0001c0001t0007g0077a0001c0001t0008g0009a0001c0001t0008g0072others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1932_193+1935d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | |||||
| chr1:66942046
|
T | G | 1 | a0001c0001t0007g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.193+1994T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942046 | ||||||
| chr1:66942158
|
A | G | 1 | a0001c0001t0007g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193+2106A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942158 | ||||||
| chr1:66942218
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193+2166G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942218 | ||||||
| chr1:66942232
|
A | G | 1 | a0001c0001t0034g0138 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.193+2180A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942232 | ||||||
| chr1:66942671
|
A | C | 1 | a0001c0001t0002g0195 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.193+2619A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942671 | ||||||
| chr1:66942763
|
G | A | 1 | a0001c0001t0005g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193+2711G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942763 | ||||||
| chr1:66942771
|
G | A | 2 | a0001c0001t0004g0026a0001c0001t0010g0018 | 2 | HG01934.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.193+2719G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942771 | ||||||
| chr1:66942990
|
T | C | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2938T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942990 | ||||||
| chr1:66943145
|
A | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.194-3005A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943145 | ||||||
| chr1:66943224
|
A | T | 1 | a0001c0001t0011g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-2926A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943224 | ||||||
| chr1:66943614
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.194-2536C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943614 | ||||||
| chr1:66943633
|
T | A | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.194-2517T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943633 | ||||||
| chr1:66943662
|
C | T | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.194-2488C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943662 | ||||||
| chr1:66943876
|
A | G | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-2274A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943876 | ||||||
| chr1:66943990
|
AT | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.194-2148delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66943990 | |||||
| chr1:66944131
|
AATT | A | 3 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223 | 3 | HG01243.hp2 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.194-2015_194-2013d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944131 | |||||
| chr1:66944303
|
TA | T | 22 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0030others(19): Show | 24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.194-1842delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944303 | |||||
| chr1:66944355
|
C | T | 27 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.194-1795C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944355 | ||||||
| chr1:66944371
|
CTAGGTCC others(35): Show |
C | 1 | a0001c0001t0001g0136 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.194-1775_194-1734d others(44): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944371 | |||||
| chr1:66944488
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.194-1662A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944488 | ||||||
| chr1:66944590
|
A | AT | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.194-1558dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944590 | |||||
| chr1:66944721
|
T | A | 4 | a0001c0001t0002g0197a0001c0002t0015g0048a0001c0002t0015g0049others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-1429T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944721 | ||||||
| chr1:66945260
|
G | GGT | 6 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(3): Show | 6 | HG00423.hp2 HG01943.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-883_194-882dup others(2): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945260 | |||||
| chr1:66945267
|
G | GTGTATAT others(1): Show |
3 | a0001c0001t0003g0227a0001c0001t0018g0209a0001c0001t0018g0228 | 3 | NA18967.hp1 NA19003.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.194-882_194-881ins others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0027g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.194-882_194-881ins others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATA | G | 5 | a0001c0001t0003g0191a0001c0001t0003g0207a0001c0001t0003g0208others(2): Show | 5 | HG00323.hp2 HG01261.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-836_194-833del others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATA | G | 8 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0195others(5): Show | 8 | HG01516.hp2 HG01517.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-838_194-833del others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(1): Show |
G | 4 | a0001c0001t0002g0014a0001c0001t0002g0187a0001c0001t0002g0213others(1): Show | 5 | HG01496.hp1 NA18954.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-840_194-833del others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(3): Show |
G | 5 | a0001c0001t0002g0186a0001c0001t0002g0197a0001c0001t0003g0013others(2): Show | 6 | HG00558.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-842_194-833del others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0002g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.194-844_194-833del others(12): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(7): Show |
G | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0028g0181 | 3 | HG00639.hp2 HG02300.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.194-846_194-833del others(14): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(13): Show |
G | 3 | a0001c0001t0004g0027a0001c0001t0010g0025a0001c0001t0024g0017 | 3 | HG02559.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.194-852_194-833del others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(15): Show |
G | 18 | a0001c0001t0001g0154a0001c0001t0004g0015a0001c0001t0004g0022others(15): Show | 20 | HG01255.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.194-854_194-833del others(22): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(17): Show |
G | 11 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0005g0037others(8): Show | 11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.194-856_194-833del others(24): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(19): Show |
G | 27 | a0001c0001t0001g0152a0001c0001t0002g0180a0001c0001t0002g0198others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.194-858_194-833del others(26): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(21): Show |
G | 6 | a0001c0001t0001g0151a0001c0001t0006g0135a0001c0001t0033g0150others(3): Show | 6 | HG01109.hp2 HG02129.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-860_194-833del others(28): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945267
|
GTATATAT others(23): Show |
G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(112): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.194-862_194-833del others(30): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | |||||
| chr1:66945269
|
A | G | 4 | a0001c0001t0003g0219a0001c0001t0003g0224a0001c0001t0004g0058others(1): Show | 4 | HG01167.hp1 HG03139.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-881A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945269 | ||||||
| chr1:66945271
|
A | G | 2 | a0001c0001t0003g0205a0001c0001t0003g0221 | 2 | HG01243.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.194-879A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945271 | ||||||
| chr1:66945273
|
A | G | 4 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0216others(1): Show | 4 | HG01261.hp1 HG02129.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-877A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945273 | ||||||
| chr1:66945279
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0206 | 3 | HG00558.hp2 NA18995.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.194-871A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945279 | ||||||
| chr1:66945289
|
A | G | 3 | a0001c0001t0004g0027a0001c0001t0010g0025a0001c0001t0024g0017 | 3 | HG02559.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.194-861A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945289 | ||||||
| chr1:66945291
|
A | G | 18 | a0001c0001t0001g0154a0001c0001t0004g0015a0001c0001t0004g0022others(15): Show | 20 | HG01255.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.194-859A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945291 | ||||||
| chr1:66945291
|
ATATATAT others(23): Show |
A | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-858_194-829del others(30): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945291 | ||||||
| chr1:66945292
|
TATATATA others(19): Show |
T | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.194-856_194-831del others(26): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945292 | |||||
| chr1:66945293
|
A | G | 11 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0005g0037others(8): Show | 11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.194-857A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945293 | ||||||
| chr1:66945295
|
A | G | 20 | a0001c0001t0001g0152a0001c0001t0004g0004a0001c0001t0004g0008others(17): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.194-855A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945295 | ||||||
| chr1:66945297
|
A | G | 6 | a0001c0001t0001g0151a0001c0001t0006g0135a0001c0001t0033g0150others(3): Show | 6 | HG01109.hp2 HG02129.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-853A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945297 | ||||||
| chr1:66945299
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(112): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.194-851A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945299 | ||||||
| chr1:66945308
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0026g0171a0001c0001t0035g0175 | 2 | HG01192.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.194-840_194-831del others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945308 | |||||
| chr1:66945316
|
T | A | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0027g0220 | 3 | HG00423.hp2 HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.194-834T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945316 | ||||||
| chr1:66945318
|
A | T | 1 | a0001c0001t0013g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194-832A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945318 | ||||||
| chr1:66945323
|
C | A | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-827C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945323 | ||||||
| chr1:66945324
|
C | A | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-826C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945324 | ||||||
| chr1:66945374
|
T | G | 14 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(11): Show | 14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-776T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945374 | ||||||
| chr1:66945478
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.194-672C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945478 | ||||||
| chr1:66945501
|
T | C | 1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.194-649T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945501 | ||||||
| chr1:66945545
|
G | A | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.194-605G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945545 | ||||||
| chr1:66945641
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.194-509T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945641 | ||||||
| chr1:66945909
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0006g0001a0001c0001t0006g0113others(2): Show | 7 | HG00423.hp1 HG01106.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-241T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945909 | ||||||
| chr1:66945973
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0157 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.194-177C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945973 | ||||||
| chr1:66946017
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02027.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.194-133A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66946017 | ||||||
| chr1:66946402
|
T | C | 1 | a0001c0001t0003g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.339+107T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946402 | ||||||
| chr1:66946436
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+141G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946436 | ||||||
| chr1:66946552
|
G | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.339+257G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946552 | ||||||
| chr1:66946578
|
G | T | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.339+283G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946578 | ||||||
| chr1:66946584
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02080.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.339+289A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946584 | ||||||
| chr1:66946685
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.339+390A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946685 | ||||||
| chr1:66946828
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+533A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946828 | ||||||
| chr1:66946936
|
TC | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+643delC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66946936 | |||||
| chr1:66946967
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.339+672T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946967 | ||||||
| chr1:66947040
|
T | A | 1 | a0001c0001t0033g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.339+745T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947040 | ||||||
| chr1:66947139
|
T | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(173): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.339+844T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947139 | ||||||
| chr1:66947231
|
G | T | 1 | a0003c0006t0004g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.339+936G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947231 | ||||||
| chr1:66947235
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.339+940G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947235 | ||||||
| chr1:66947270
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.339+975C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947270 | ||||||
| chr1:66947308
|
C | G | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+1013C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947308 | ||||||
| chr1:66947368
|
A | G | 1 | a0001c0001t0019g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.339+1073A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947368 | ||||||
| chr1:66947489
|
A | G | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+1194A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947489 | ||||||
| chr1:66947792
|
C | T | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+1497C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947792 | ||||||
| chr1:66947794
|
C | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0165 | 3 | HG01891.hp1 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.339+1499C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947794 | ||||||
| chr1:66947795
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.339+1500A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947795 | ||||||
| chr1:66947902
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+1607G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947902 | ||||||
| chr1:66947935
|
C | T | 25 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(22): Show | 26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+1640C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947935 | ||||||
| chr1:66948038
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0097others(24): Show | 28 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.339+1743A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948038 | ||||||
| chr1:66948067
|
G | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.339+1772G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948067 | ||||||
| chr1:66948431
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.339+2136A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948431 | ||||||
| chr1:66948685
|
G | C | 3 | a0001c0001t0001g0118a0002c0003t0001g0119a0002c0003t0006g0137 | 3 | HG00323.hp1 HG00738.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.339+2390G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948685 | ||||||
| chr1:66949108
|
G | T | 3 | a0001c0001t0005g0045a0001c0001t0005g0046a0001c0001t0005g0047 | 3 | HG01106.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.339+2813G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949108 | ||||||
| chr1:66949187
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.339+2892G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949187 | ||||||
| chr1:66949334
|
G | T | 1 | a0001c0001t0005g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+3039G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949334 | ||||||
| chr1:66949335
|
C | G | 1 | a0001c0001t0005g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+3040C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949335 | ||||||
| chr1:66949546
|
C | A | 1 | a0001c0001t0004g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339+3251C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949546 | ||||||
| chr1:66949936
|
AC | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.339+3642delC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949936 | ||||||
| chr1:66949963
|
ATTG | A | 6 | a0001c0001t0008g0009a0001c0001t0008g0071a0001c0001t0008g0072others(3): Show | 7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+3671_339+3673d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66949963 | |||||
| chr1:66950004
|
T | C | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+3709T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950004 | ||||||
| chr1:66950094
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0033g0150 | 2 | HG01109.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.339+3799A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950094 | ||||||
| chr1:66950213
|
A | T | 5 | a0001c0001t0008g0009a0001c0001t0008g0072a0001c0001t0008g0073others(2): Show | 6 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+3918A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950213 | ||||||
| chr1:66950389
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+4094G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950389 | ||||||
| chr1:66950407
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.339+4112C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950407 | ||||||
| chr1:66950418
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(224): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.339+4123T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950418 | ||||||
| chr1:66950709
|
A | AC | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(180): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.339+4414_339+4415i others(3): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950709 | ||||||
| chr1:66950713
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.339+4418A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950713 | ||||||
| chr1:66950749
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.339+4454T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950749 | ||||||
| chr1:66950838
|
ATC | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.339+4549_339+4550d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66950838 | |||||
| chr1:66950910
|
A | G | 1 | a0001c0001t0013g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.339+4615A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950910 | ||||||
| chr1:66951256
|
G | A | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+4961G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951256 | ||||||
| chr1:66951294
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.339+4999A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951294 | ||||||
| chr1:66951418
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(173): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.339+5123T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951418 | ||||||
| chr1:66951428
|
C | T | 2 | a0001c0001t0007g0083a0001c0001t0017g0082 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.339+5133C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951428 | ||||||
| chr1:66951494
|
A | G | 2 | a0001c0001t0016g0084a0001c0001t0016g0092 | 2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.339+5199A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951494 | ||||||
| chr1:66951558
|
T | C | 1 | a0001c0001t0029g0178 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.339+5263T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951558 | ||||||
| chr1:66951572
|
GT | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(174): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.339+5289delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66951572 | |||||
| chr1:66951767
|
C | T | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.339+5472C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951767 | ||||||
| chr1:66951838
|
T | C | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.339+5543T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951838 | ||||||
| chr1:66951872
|
G | T | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+5577G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951872 | ||||||
| chr1:66951951
|
C | T | 5 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0177others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+5656C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951951 | ||||||
| chr1:66952059
|
A | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.339+5764A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952059 | ||||||
| chr1:66952074
|
CTTAG | C | 2 | a0001c0001t0014g0007a0001c0001t0014g0040 | 3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.339+5783_339+5786d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66952074 | |||||
| chr1:66952344
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.340-5715C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952344 | ||||||
| chr1:66952432
|
A | G | 25 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(22): Show | 26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-5627A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952432 | ||||||
| chr1:66952637
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.340-5422A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952637 | ||||||
| chr1:66952758
|
C | T | 1 | a0001c0001t0006g0132 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.340-5301C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952758 | ||||||
| chr1:66952779
|
C | T | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.340-5280C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952779 | ||||||
| chr1:66953122
|
T | G | 1 | a0001c0001t0007g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.340-4937T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953122 | ||||||
| chr1:66953184
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.340-4875G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953184 | ||||||
| chr1:66953406
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.340-4653G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953406 | ||||||
| chr1:66953596
|
C | CT | 13 | a0001c0001t0001g0112a0001c0001t0003g0216a0001c0001t0003g0217others(10): Show | 13 | HG00423.hp2 HG01243.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.340-4447dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66953596 | |||||
| chr1:66953612
|
T | TA | 25 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(22): Show | 26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-4445dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66953612 | |||||
| chr1:66953777
|
T | A | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340-4282T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953777 | ||||||
| chr1:66953818
|
G | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.340-4241G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953818 | ||||||
| chr1:66953834
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(203): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.340-4225T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953834 | ||||||
| chr1:66954238
|
G | A | 1 | a0001c0001t0013g0176 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-3821G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954238 | ||||||
| chr1:66954483
|
G | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.340-3576G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954483 | ||||||
| chr1:66954548
|
C | T | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-3511C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954548 | ||||||
| chr1:66954553
|
C | G | 1 | a0001c0001t0003g0202 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.340-3506C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954553 | ||||||
| chr1:66954852
|
G | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-3207G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954852 | ||||||
| chr1:66954908
|
C | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.340-3151C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954908 | ||||||
| chr1:66954995
|
C | T | 25 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(22): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.340-3064C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954995 | ||||||
| chr1:66955336
|
G | GT | 51 | a0001c0001t0001g0103a0001c0001t0001g0118a0001c0001t0001g0120others(48): Show | 53 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.340-2695dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | |||||
| chr1:66955336
|
G | GTT | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(97): Show | 109 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.340-2696_340-2695d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | |||||
| chr1:66955336
|
G | GTTT | 38 | a0001c0001t0001g0010a0001c0001t0001g0098a0001c0001t0001g0112others(35): Show | 40 | HG00140.hp1 HG00621.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-2697_340-2695d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | |||||
| chr1:66955336
|
GT | G | 5 | a0001c0001t0002g0180a0001c0001t0002g0187a0001c0001t0002g0213others(2): Show | 5 | HG00323.hp2 HG02895.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-2695delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | |||||
| chr1:66955336
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340-2706_340-2695d others(14): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | |||||
| chr1:66955546
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.340-2513A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955546 | ||||||
| chr1:66955628
|
A | G | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-2431A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955628 | ||||||
| chr1:66955707
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.340-2352C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955707 | ||||||
| chr1:66955769
|
G | A | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-2290G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955769 | ||||||
| chr1:66955795
|
G | T | 1 | a0001c0001t0002g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.340-2264G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955795 | ||||||
| chr1:66956031
|
G | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(181): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.340-2028G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956031 | ||||||
| chr1:66956236
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.340-1823A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956236 | ||||||
| chr1:66956324
|
G | T | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-1735G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956324 | ||||||
| chr1:66956618
|
T | C | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-1441T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956618 | ||||||
| chr1:66956830
|
A | G | 1 | a0001c0001t0007g0078 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.340-1229A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956830 | ||||||
| chr1:66956867
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.340-1192C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956867 | ||||||
| chr1:66957217
|
A | G | 1 | a0001c0001t0009g0129 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.340-842A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957217 | ||||||
| chr1:66957307
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(203): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.340-752C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957307 | ||||||
| chr1:66957405
|
ATGCTTAA others(2): Show |
A | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.340-651_340-643del others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957405 | |||||
| chr1:66957557
|
A | G | 1 | a0001c0001t0019g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.340-502A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957557 | ||||||
| chr1:66957587
|
G | GT | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0087others(37): Show | 41 | HG00597.hp1 HG00621.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.340-452dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957587 | |||||
| chr1:66957631
|
AT | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.340-424delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957631 | |||||
| chr1:66958314
|
T | TTTCTC | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.501+97_501+98insTC others(3): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958314 | |||||
| chr1:66958447
|
T | TATTCTTT others(314): Show |
1 | a0001c0001t0007g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.501+232_501+233ins others(321): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958447 | |||||
| chr1:66958474
|
TA | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(175): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.501+261delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958474 | |||||
| chr1:66958589
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0158 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-262C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958589 | ||||||
| chr1:66958805
|
A | G | 22 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0030others(19): Show | 24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-46A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958805 | ||||||
| chr1:66958835
|
A | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.502-16A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958835 | ||||||
| chr1:66959335
|
A | C | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.635-344A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 6/13 | chr1 | 66959335 | ||||||
| chr1:66959628
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.635-51T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 6/13 | chr1 | 66959628 | ||||||
| chr1:66959793
|
A | T | 3 | a0001c0001t0001g0118a0002c0003t0001g0119a0002c0003t0006g0137 | 3 | HG00323.hp1 HG00738.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.699+50A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66959793 | ||||||
| chr1:66959811
|
A | AT | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(170): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.699+79dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66959811 | |||||
| chr1:66959976
|
T | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.699+233T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66959976 | ||||||
| chr1:66960087
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.699+344G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960087 | ||||||
| chr1:66960356
|
G | A | 1 | a0001c0001t0006g0132 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.699+613G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960356 | ||||||
| chr1:66960540
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(173): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.699+797A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960540 | ||||||
| chr1:66960657
|
A | T | 14 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(11): Show | 14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.699+914A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960657 | ||||||
| chr1:66960804
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.699+1061A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960804 | ||||||
| chr1:66960912
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.699+1169A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960912 | ||||||
| chr1:66961033
|
T | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.699+1290T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961033 | ||||||
| chr1:66961227
|
T | G | 2 | a0001c0001t0002g0190a0001c0001t0003g0211 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.699+1484T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961227 | ||||||
| chr1:66961256
|
C | T | 1 | a0001c0001t0016g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.699+1513C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961256 | ||||||
| chr1:66961509
|
T | C | 1 | a0001c0001t0032g0146 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.700-1579T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961509 | ||||||
| chr1:66961623
|
G | T | 25 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(22): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.700-1465G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961623 | ||||||
| chr1:66961710
|
G | T | 1 | a0001c0001t0013g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-1378G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961710 | ||||||
| chr1:66961725
|
A | G | 2 | a0001c0001t0004g0027a0001c0001t0010g0025 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.700-1363A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961725 | ||||||
| chr1:66961864
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.700-1224A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961864 | ||||||
| chr1:66961995
|
G | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.700-1093G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961995 | ||||||
| chr1:66962086
|
C | T | 17 | a0001c0001t0005g0005a0001c0001t0005g0030a0001c0001t0005g0031others(14): Show | 18 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.700-1002C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962086 | ||||||
| chr1:66962319
|
C | CT | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.700-768dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66962319 | |||||
| chr1:66962319
|
C | G | 2 | a0001c0001t0017g0061a0001c0001t0017g0062 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.700-769C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962319 | ||||||
| chr1:66962353
|
A | G | 6 | a0001c0001t0008g0009a0001c0001t0008g0071a0001c0001t0008g0072others(3): Show | 7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-735A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962353 | ||||||
| chr1:66962457
|
A | G | 6 | a0001c0001t0009g0003a0001c0001t0009g0012a0001c0001t0009g0129others(3): Show | 9 | HG01069.hp1 HG01099.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-631A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962457 | ||||||
| chr1:66962829
|
CTTCT | C | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.700-256_700-253del others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66962829 | |||||
| chr1:66962892
|
G | C | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.700-196G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962892 | ||||||
| chr1:66963541
|
G | A | 1 | a0001c0001t0006g0113 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.772+381G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963541 | ||||||
| chr1:66963770
|
T | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.772+610T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963770 | ||||||
| chr1:66963776
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.772+616C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963776 | ||||||
| chr1:66964009
|
CCATTT | C | 3 | a0001c0001t0005g0039a0001c0001t0005g0044a0001c0001t0025g0038 | 3 | HG03654.hp2 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.772+860_772+864del others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964009 | |||||
| chr1:66964073
|
A | AT | 6 | a0001c0001t0001g0087a0001c0001t0001g0103a0001c0001t0001g0109others(3): Show | 6 | HG02698.hp1 NA18972.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+928dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964073 | |||||
| chr1:66964090
|
A | G | 27 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(24): Show | 28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.772+930A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964090 | ||||||
| chr1:66964179
|
C | G | 1 | a0001c0001t0035g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.772+1019C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964179 | ||||||
| chr1:66964348
|
C | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0229a0001c0001t0022g0100others(1): Show | 4 | HG00597.hp2 NA18960.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.772+1188C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964348 | ||||||
| chr1:66964420
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+1260G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964420 | ||||||
| chr1:66964448
|
CT | C | 8 | a0001c0001t0002g0182a0001c0001t0013g0172a0001c0001t0013g0176others(5): Show | 8 | HG01167.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+1309delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964448 | |||||
| chr1:66964448
|
CTTTTTT | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(170): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.772+1304_772+1309d others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964448 | |||||
| chr1:66964671
|
T | TG | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.772+1512dupG | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964671 | |||||
| chr1:66964744
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+1584A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964744 | ||||||
| chr1:66964812
|
A | G | 1 | a0001c0001t0013g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.772+1652A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964812 | ||||||
| chr1:66965157
|
G | A | 2 | a0001c0001t0005g0041a0001c0001t0005g0042 | 2 | NA18988.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.772+1997G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965157 | ||||||
| chr1:66965206
|
C | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.772+2046C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965206 | ||||||
| chr1:66965275
|
A | G | 2 | a0001c0001t0005g0006a0001c0001t0012g0006 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.772+2115A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965275 | ||||||
| chr1:66965682
|
A | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+2522A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965682 | ||||||
| chr1:66965691
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | NA18971.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.772+2531T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965691 | ||||||
| chr1:66965816
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+2656T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965816 | ||||||
| chr1:66966040
|
A | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.772+2880A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966040 | ||||||
| chr1:66966225
|
C | T | 1 | a0001c0001t0006g0132 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.772+3065C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966225 | ||||||
| chr1:66966261
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.772+3101C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966261 | ||||||
| chr1:66966304
|
C | A | 1 | a0001c0001t0003g0224 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.772+3144C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966304 | ||||||
| chr1:66966312
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.772+3152T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966312 | ||||||
| chr1:66966348
|
C | T | 57 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(54): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.772+3188C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966348 | ||||||
| chr1:66966385
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0090a0001c0001t0016g0092 | 3 | HG02738.hp2 HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.772+3225A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966385 | ||||||
| chr1:66967200
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.773-3608G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967200 | ||||||
| chr1:66967302
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.773-3506T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967302 | ||||||
| chr1:66967402
|
G | T | 3 | a0001c0001t0003g0204a0001c0001t0003g0210a0001c0001t0018g0209 | 3 | NA18990.hp1 NA18991.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.773-3406G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967402 | ||||||
| chr1:66967510
|
CT | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | NA18971.hp2 NA19003.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-3291delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66967510 | |||||
| chr1:66967644
|
AT | A | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-3150delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66967644 | |||||
| chr1:66967685
|
A | G | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.773-3123A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967685 | ||||||
| chr1:66967816
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.773-2992A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967816 | ||||||
| chr1:66967986
|
A | C | 1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.773-2822A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967986 | ||||||
| chr1:66968100
|
C | T | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.773-2708C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968100 | ||||||
| chr1:66968591
|
C | T | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773-2217C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968591 | ||||||
| chr1:66968712
|
A | G | 1 | a0001c0001t0007g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.773-2096A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968712 | ||||||
| chr1:66968728
|
A | G | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-2080A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968728 | ||||||
| chr1:66968801
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.773-2007G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968801 | ||||||
| chr1:66968919
|
C | T | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-1889C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968919 | ||||||
| chr1:66969140
|
T | C | 1 | a0001c0001t0030g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.773-1668T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969140 | ||||||
| chr1:66969267
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773-1541C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969267 | ||||||
| chr1:66969296
|
A | G | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773-1512A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969296 | ||||||
| chr1:66969312
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.773-1496G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969312 | ||||||
| chr1:66969479
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.773-1329A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969479 | ||||||
| chr1:66969495
|
A | G | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.773-1313A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969495 | ||||||
| chr1:66969502
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.773-1306G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969502 | ||||||
| chr1:66969545
|
C | CA | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0086others(8): Show | 12 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.773-1233dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
C | CAA | 17 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0098others(14): Show | 17 | HG01934.hp2 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.773-1234_773-1233d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CA | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0099others(43): Show | 51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-1233delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAA | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0183a0001c0001t0002g0187others(32): Show | 36 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.773-1234_773-1233d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAAA | C | 31 | a0001c0001t0003g0013a0001c0001t0003g0179a0001c0001t0003g0210others(28): Show | 33 | HG00423.hp2 HG00558.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.773-1235_773-1233d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAAAA | C | 54 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0016others(51): Show | 57 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.773-1236_773-1233d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAAAAA | C | 6 | a0001c0001t0010g0067a0001c0001t0013g0172a0001c0001t0013g0173others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-1237_773-1233d others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0166others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-1243_773-1233d others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969545
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0186a0001c0001t0020g0225a0001c0001t0020g0226 | 3 | HG02257.hp1 HG02723.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.773-1245_773-1233d others(15): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | |||||
| chr1:66969581
|
G | C | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-1227G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969581 | ||||||
| chr1:66969730
|
A | G | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.773-1078A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969730 | ||||||
| chr1:66969928
|
T | G | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.773-880T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969928 | ||||||
| chr1:66969934
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.773-874A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969934 | ||||||
| chr1:66970089
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0121 | 2 | NA18953.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.773-719T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970089 | ||||||
| chr1:66970098
|
AT | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.773-708delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66970098 | |||||
| chr1:66970223
|
C | G | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773-585C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970223 | ||||||
| chr1:66970573
|
A | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.773-235A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970573 | ||||||
| chr1:66970613
|
A | G | 1 | a0001c0001t0006g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.773-195A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970613 | ||||||
| chr1:66970763
|
A | G | 31 | a0001c0001t0002g0014a0001c0001t0002g0182a0001c0001t0002g0183others(28): Show | 32 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.773-45A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970763 | ||||||
| chr1:66971262
|
T | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.924+303T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971262 | ||||||
| chr1:66971351
|
T | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.925-304T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971351 | ||||||
| chr1:66971360
|
C | T | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.925-295C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971360 | ||||||
| chr1:66971404
|
C | A | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.925-251C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971404 | ||||||
| chr1:66971467
|
A | G | 3 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0026g0171 | 3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.925-188A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971467 | ||||||
| chr1:66971890
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0017g0061 | 2 | HG02622.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1006+154C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66971890 | ||||||
| chr1:66972050
|
GATA | G | 55 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(52): Show | 57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1006+318_1006+320d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972050 | |||||
| chr1:66972151
|
C | A | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1006+415C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972151 | ||||||
| chr1:66972216
|
C | CAT | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1006+492_1006+493d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972216 | |||||
| chr1:66972228
|
TACACTAC | T | 5 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+494_1006+500d others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972228 | |||||
| chr1:66972229
|
ACAC | A | 49 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(46): Show | 51 | HG00558.hp2 HG00639.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1006+494_1006+496d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972229 | ||||||
| chr1:66972232
|
CTACATAT others(7): Show |
C | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+499_1006+512d others(16): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972232 | |||||
| chr1:66972235
|
C | CAT | 9 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0128others(6): Show | 9 | HG00323.hp1 HG00597.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+525_1006+526d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | |||||
| chr1:66972235
|
C | CATAT | 4 | a0001c0001t0006g0096a0001c0001t0007g0078a0001c0004t0001g0095others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+523_1006+526d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | |||||
| chr1:66972235
|
C | CATATATA others(3): Show |
1 | a0001c0002t0015g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1006+517_1006+526d others(12): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | |||||
| chr1:66972236
|
ATATATAT | A | 43 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(40): Show | 45 | HG00558.hp2 HG00639.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006+501_1006+507d others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972236 | ||||||
| chr1:66972236
|
ATATATAT others(2): Show |
A | 3 | a0001c0001t0013g0176a0001c0001t0013g0177a0001c0001t0027g0220 | 3 | HG02132.hp1 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1006+501_1006+509d others(11): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972236 | ||||||
| chr1:66972239
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1006+522_1006+523i others(27): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972239 | |||||
| chr1:66972240
|
A | C | 1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1006+504A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972240 | ||||||
| chr1:66972241
|
T | C | 5 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+505T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972241 | ||||||
| chr1:66972242
|
A | C | 2 | a0001c0001t0002g0187a0001c0001t0003g0179 | 2 | HG03017.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1006+506A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972242 | ||||||
| chr1:66972242
|
AT | A | 5 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+507delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972242 | ||||||
| chr1:66972243
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1006+507T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972243 | ||||||
| chr1:66972244
|
A | C | 48 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(45): Show | 50 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1006+508A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972244 | ||||||
| chr1:66972245
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0005g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1006+514_1006+531d others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972245 | |||||
| chr1:66972246
|
A | C | 4 | a0001c0001t0003g0217a0001c0001t0013g0176a0001c0001t0013g0177others(1): Show | 4 | HG00423.hp2 HG02132.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+510A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972246 | ||||||
| chr1:66972257
|
TATATAG | T | 10 | a0001c0001t0005g0043a0001c0001t0007g0064a0001c0001t0008g0009others(7): Show | 11 | HG00735.hp2 HG02615.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+526_1006+531d others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972257 | |||||
| chr1:66972259
|
TATAG | T | 73 | a0001c0001t0001g0011a0001c0001t0001g0085a0001c0001t0001g0086others(70): Show | 77 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1006+527_1006+530d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972259 | |||||
| chr1:66972261
|
TAG | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0091others(21): Show | 24 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006+527_1006+528d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972261 | |||||
| chr1:66972263
|
G | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0163others(70): Show | 75 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1006+527G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972263 | ||||||
| chr1:66972455
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1007-442C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972455 | ||||||
| chr1:66972809
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1007-88C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972809 | ||||||
| chr1:66972852
|
A | T | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1007-45A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972852 | ||||||
| chr1:66973217
|
G | A | 57 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(54): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1101+226G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973217 | ||||||
| chr1:66973375
|
T | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1101+384T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973375 | ||||||
| chr1:66973407
|
G | C | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1101+416G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973407 | ||||||
| chr1:66973410
|
G | C | 22 | a0001c0001t0003g0013a0001c0001t0003g0179a0001c0001t0003g0202others(19): Show | 23 | HG00423.hp2 HG00558.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1101+419G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973410 | ||||||
| chr1:66973437
|
C | T | 8 | a0001c0001t0008g0009a0001c0001t0008g0051a0001c0001t0008g0052others(5): Show | 9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+446C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973437 | ||||||
| chr1:66973833
|
T | C | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1101+842T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973833 | ||||||
| chr1:66974002
|
A | T | 1 | a0001c0001t0002g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1101+1011A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974002 | ||||||
| chr1:66974067
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1101+1076C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974067 | ||||||
| chr1:66974385
|
C | T | 8 | a0001c0001t0008g0009a0001c0001t0008g0051a0001c0001t0008g0052others(5): Show | 9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+1394C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974385 | ||||||
| chr1:66974433
|
T | G | 4 | a0001c0001t0002g0196a0001c0002t0015g0048a0001c0002t0015g0049others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1442T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974433 | ||||||
| chr1:66974436
|
G | T | 48 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(45): Show | 51 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.1101+1445G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974436 | ||||||
| chr1:66974439
|
G | T | 1 | a0001c0001t0014g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1101+1448G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974439 | ||||||
| chr1:66974539
|
T | C | 25 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(22): Show | 26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1101+1548T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974539 | ||||||
| chr1:66974540
|
G | A | 2 | a0001c0001t0007g0064a0001c0001t0007g0065 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1101+1549G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974540 | ||||||
| chr1:66974779
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0157 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1101+1788C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974779 | ||||||
| chr1:66974800
|
C | A | 25 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(22): Show | 26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1102-1795C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974800 | ||||||
| chr1:66975019
|
G | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102-1576G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975019 | ||||||
| chr1:66975113
|
C | T | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102-1482C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975113 | ||||||
| chr1:66975164
|
A | G | 4 | a0001c0001t0001g0123a0001c0001t0001g0140a0001c0001t0001g0164others(1): Show | 4 | HG03669.hp2 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-1431A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975164 | ||||||
| chr1:66975444
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1102-1151T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975444 | ||||||
| chr1:66975533
|
A | G | 1 | a0001c0001t0004g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1102-1062A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975533 | ||||||
| chr1:66975538
|
AAAAG | A | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1102-1052_1102-104 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975538 | |||||
| chr1:66975679
|
C | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1102-916C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975679 | ||||||
| chr1:66975923
|
A | G | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-672A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975923 | ||||||
| chr1:66975983
|
C | CT | 7 | a0001c0001t0004g0058a0001c0001t0004g0059a0001c0001t0005g0006others(4): Show | 8 | HG01167.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-604dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975983 | |||||
| chr1:66975988
|
T | G | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1102-607T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975988 | ||||||
| chr1:66975988
|
T | TTG | 53 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(50): Show | 55 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1102-606_1102-605i others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975988 | |||||
| chr1:66975990
|
T | G | 59 | a0001c0001t0001g0112a0001c0001t0001g0134a0001c0001t0002g0014others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1102-605T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975990 | ||||||
| chr1:66975992
|
G | T | 72 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(69): Show | 76 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1102-603G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975992 | ||||||
| chr1:66976018
|
C | T | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-577C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976018 | ||||||
| chr1:66976032
|
G | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102-563G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976032 | ||||||
| chr1:66976245
|
A | AC | 27 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(24): Show | 28 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1102-344dupC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66976245 | |||||
| chr1:66976527
|
C | T | 49 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(46): Show | 51 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1102-68C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976527 | ||||||
| chr1:66976539
|
A | C | 1 | a0001c0001t0008g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1102-56A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976539 | ||||||
| chr1:66976567
|
CT | C | 16 | a0001c0001t0004g0004a0001c0001t0004g0015a0001c0001t0004g0016others(13): Show | 17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1102-26delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66976567 | |||||
| chr1:66976592
|
C | T | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.1102-3C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976592 | ||||||
| chr1:66976888
|
C | G | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+166C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66976888 | ||||||
| chr1:66977060
|
T | C | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1229+338T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977060 | ||||||
| chr1:66977116
|
T | C | 1 | a0001c0001t0033g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1229+394T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977116 | ||||||
| chr1:66977202
|
C | T | 3 | a0001c0001t0021g0068a0001c0001t0021g0070a0001c0001t0031g0069 | 3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1229+480C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977202 | ||||||
| chr1:66977213
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1229+491G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977213 | ||||||
| chr1:66977630
|
T | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1229+908T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977630 | ||||||
| chr1:66977982
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1229+1260A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977982 | ||||||
| chr1:66978068
|
C | G | 55 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(52): Show | 57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1229+1346C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978068 | ||||||
| chr1:66978209
|
A | AAAAG | 55 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(52): Show | 57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1229+1489_1229+149 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978209 | |||||
| chr1:66978209
|
A | G | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+1487A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978209 | ||||||
| chr1:66978286
|
ATAGG | A | 58 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(55): Show | 60 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1229+1571_1229+157 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978286 | |||||
| chr1:66978305
|
G | C | 2 | a0001c0001t0029g0178a0001c0001t0030g0174 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+1583G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978305 | ||||||
| chr1:66978360
|
G | A | 27 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(24): Show | 28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1229+1638G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978360 | ||||||
| chr1:66978402
|
A | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0159 | 3 | NA18971.hp2 NA19003.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1229+1680A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978402 | ||||||
| chr1:66978442
|
AT | A | 3 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223 | 3 | HG01243.hp2 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1229+1722delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978442 | |||||
| chr1:66978681
|
C | CATTATTC others(9): Show |
1 | a0001c0001t0005g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1229+1959_1229+196 others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978681 | ||||||
| chr1:66978807
|
G | T | 11 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0041others(8): Show | 11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.1229+2085G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978807 | ||||||
| chr1:66979081
|
G | T | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1229+2359G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979081 | ||||||
| chr1:66979097
|
G | GT | 4 | a0001c0001t0005g0006a0001c0001t0012g0006a0001c0001t0014g0007others(1): Show | 5 | HG02451.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1229+2385dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66979097 | |||||
| chr1:66979100
|
T | C | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1229+2378T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979100 | ||||||
| chr1:66979113
|
G | A | 1 | a0001c0001t0004g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1229+2391G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979113 | ||||||
| chr1:66979156
|
C | T | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1229+2434C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979156 | ||||||
| chr1:66979280
|
G | T | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1230-2499G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979280 | ||||||
| chr1:66979340
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1230-2439C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979340 | ||||||
| chr1:66979638
|
T | C | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1230-2141T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979638 | ||||||
| chr1:66979784
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1230-1995C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979784 | ||||||
| chr1:66979880
|
G | A | 1 | a0001c0001t0006g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1230-1899G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979880 | ||||||
| chr1:66980294
|
T | C | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1230-1485T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980294 | ||||||
| chr1:66980371
|
C | T | 6 | a0001c0001t0008g0009a0001c0001t0008g0071a0001c0001t0008g0072others(3): Show | 7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230-1408C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980371 | ||||||
| chr1:66980439
|
T | C | 3 | a0001c0001t0011g0145a0001c0001t0011g0155a0001c0001t0011g0162 | 3 | HG01934.hp2 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1230-1340T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980439 | ||||||
| chr1:66980684
|
T | A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1230-1095T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980684 | ||||||
| chr1:66980812
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1230-967A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980812 | ||||||
| chr1:66981003
|
C | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1230-776C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981003 | ||||||
| chr1:66981009
|
T | A | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-770T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981009 | ||||||
| chr1:66981010
|
T | A | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-769T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981010 | ||||||
| chr1:66981011
|
T | A | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-768T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981011 | ||||||
| chr1:66981013
|
T | G | 6 | a0001c0001t0013g0172a0001c0001t0013g0173a0001c0001t0013g0176others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-766T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981013 | ||||||
| chr1:66981087
|
T | TTAGA | 141 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0166others(138): Show | 147 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.1230-691_1230-688d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66981087 | |||||
| chr1:66981253
|
A | AC | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1230-524dupC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66981253 | |||||
| chr1:66981306
|
G | A | 1 | a0001c0001t0035g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1230-473G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981306 | ||||||
| chr1:66981367
|
C | G | 5 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0079others(2): Show | 5 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230-412C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981367 | ||||||
| chr1:66981519
|
A | G | 1 | a0002c0003t0006g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1230-260A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981519 | ||||||
| chr1:66981540
|
T | C | 1 | a0001c0001t0014g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1230-239T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981540 | ||||||
| chr1:66981767
|
A | G | 57 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(54): Show | 59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1230-12A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981767 | ||||||
| chr1:66982005
|
T | G | 1 | a0001c0001t0020g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1369+87T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982005 | ||||||
| chr1:66982118
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1369+200A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982118 | ||||||
| chr1:66982126
|
C | G | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1369+208C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982126 | ||||||
| chr1:66982146
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1369+228T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982146 | ||||||
| chr1:66982309
|
AGTGCACT others(4): Show |
A | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1369+392_1369+402d others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982309 | ||||||
| chr1:66982335
|
C | T | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369+417C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982335 | ||||||
| chr1:66982362
|
A | G | 1 | a0001c0001t0016g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1369+444A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982362 | ||||||
| chr1:66982388
|
A | G | 3 | a0001c0002t0015g0048a0001c0002t0015g0049a0001c0002t0015g0050 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1369+470A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982388 | ||||||
| chr1:66982410
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1369+492G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982410 | ||||||
| chr1:66982740
|
CAT | C | 3 | a0001c0001t0003g0219a0001c0001t0003g0227a0001c0001t0018g0228 | 3 | NA18967.hp1 NA18975.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1369+823_1369+824d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982740 | ||||||
| chr1:66982745
|
G | A | 1 | a0001c0001t0007g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1369+827G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982745 | ||||||
| chr1:66982767
|
T | C | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1369+849T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982767 | ||||||
| chr1:66982801
|
T | A | 49 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0015others(46): Show | 52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1369+883T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982801 | ||||||
| chr1:66982853
|
C | T | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369+935C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982853 | ||||||
| chr1:66982951
|
T | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1369+1033T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982951 | ||||||
| chr1:66983050
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1369+1132A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983050 | ||||||
| chr1:66983162
|
AAAGG | A | 15 | a0001c0001t0004g0004a0001c0001t0004g0015a0001c0001t0004g0016others(12): Show | 16 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+1255_1369+125 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983162 | |||||
| chr1:66983209
|
A | G | 1 | a0001c0001t0005g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1369+1291A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983209 | ||||||
| chr1:66983313
|
A | G | 27 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(24): Show | 28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-1259A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983313 | ||||||
| chr1:66983337
|
T | G | 27 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(24): Show | 28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-1235T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983337 | ||||||
| chr1:66983395
|
A | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0036 | 2 | NA18980.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1370-1177A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983395 | ||||||
| chr1:66983479
|
ACTT | A | 24 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(21): Show | 25 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1370-1089_1370-108 others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983479 | |||||
| chr1:66983523
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1370-1049A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983523 | ||||||
| chr1:66983632
|
AT | A | 22 | a0001c0001t0007g0060a0001c0001t0007g0063a0001c0001t0007g0064others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1370-937delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983632 | |||||
| chr1:66983770
|
C | G | 1 | a0001c0001t0005g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1370-802C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983770 | ||||||
| chr1:66983779
|
A | G | 138 | a0001c0001t0001g0110a0001c0001t0001g0160a0001c0001t0001g0161others(135): Show | 144 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1370-793A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983779 | ||||||
| chr1:66983990
|
C | T | 21 | a0001c0001t0007g0060a0001c0001t0007g0064a0001c0001t0007g0065others(18): Show | 22 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1370-582C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983990 | ||||||
| chr1:66984126
|
A | C | 1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1370-446A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984126 | ||||||
| chr1:66984258
|
A | G | 59 | a0001c0001t0002g0014a0001c0001t0002g0180a0001c0001t0002g0182others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1370-314A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984258 | ||||||
| chr1:66984307
|
C | T | 2 | a0001c0001t0020g0225a0001c0001t0020g0226 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1370-265C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984307 |