Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 339541 |
|---|---|
| ensemblid | ENSG00000198520.12 |
| hgncid | 34345 |
| symbol | ARMH1 |
| name | armadillo like helical domain containing 1 |
| refseq_nuc | NM_001145636.2 |
| refseq_prot | NP_001139108.1 |
| ensembl_nuc | ENST00000535358.6 |
| ensembl_prot | ENSP00000440524.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 44674714 |
| end | 44725591 |
| strand | + |
| ver | v1.2 |
| region | chr1:44674714-44725591 |
| region5000 | chr1:44669714-44730591 |
| regionname0 | ARMH1_chr1_44674714_44725591 |
| regionname5000 | ARMH1_chr1_44669714_44730591 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 440 | 283 | 81 | 65 | 93 | 10 | 32 | 64 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0002 | 0/0 | 440 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0003 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0004 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1323 | 280 | 81 | 64 | 92 | 9 | 32 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| c0002 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| c0003 | 0/0 | 1323 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| c0004 | 0/0 | 1323 | 2 | 0 | 1 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| c0005 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| c0006 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 371 | 283 | 79 | 67 | 93 | 10 | 32 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| t0002 | 0/0 | 371 | 4 | 3 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| t0003 | 0/0 | 371 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1323 | 280 | 81 | 64 | 92 | 9 | 32 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0004 | 0/0 | 1323 | 2 | 0 | 1 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0006 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0002c0003 | 0/0 | 1323 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0003c0002 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0004c0005 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1693 | 275 | 78 | 63 | 91 | 9 | 32 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0001t0002 | 0/0 | 1693 | 4 | 3 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0001t0003 | 0/0 | 1693 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0004t0001 | 0/0 | 1693 | 2 | 0 | 1 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0001c0006t0001 | 0/0 | 1693 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0002c0003t0001 | 0/0 | 1693 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0003c0002t0001 | 0/0 | 1693 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| a0004c0005t0001 | 0/0 | 1693 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | copy fasta | chr1 | 44669714 | 44730591 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0003c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0003c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0004c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00621 | hp1 | a0004 | c0005 | t0001 | g0168 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0111 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01168 | hp2 | a0003 | c0002 | t0001 | g0136 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01175 | hp2 | a0003 | c0002 | t0001 | g0264 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0202 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01516 | hp1 | a0001 | c0006 | t0001 | g0261 | EUR | IBS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02027 | hp1 | a0001 | c0004 | t0001 | g0107 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0274 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | USA | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0263 | REF | REF | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44701045
|
G | C | 1 | a0003 | 2 | HG01168.hp2 HG01175.hp2 |
missense_variant | MODERATE | c.565G>C | p.Gly189Arg | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/12 | 747/1693 | 565/1323 | 189/440 | chr1 | 44701045 | ||
| chr1:44724139
|
G | T | 1 | a0002 | 2 | HG01243.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.742G>T | p.Asp248Tyr | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 7/12 | 924/1693 | 742/1323 | 248/440 | chr1 | 44724139 | ||
| chr1:44724166
|
G | T | 1 | a0002 | 2 | HG01243.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.769G>T | p.Ala257Ser | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 7/12 | 951/1693 | 769/1323 | 257/440 | chr1 | 44724166 | ||
| chr1:44724244
|
G | A | 1 | a0004 | 1 | HG00621.hp1 | missense_variant&splice_region_variant | MODERATE | c.847G>A | p.Asp283Asn | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 7/12 | 1029/1693 | 847/1323 | 283/440 | chr1 | 44724244 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44701011
|
C | T | 1 | a0001c0004 | 2 | HG00738.hp1 HG02027.hp1 |
synonymous_variant | LOW | c.531C>T | p.His177His | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/12 | 713/1693 | 531/1323 | 177/440 | chr1 | 44701011 | ||
| chr1:44725165
|
A | T | 1 | a0001c0006 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.1158A>T | p.Ile386Ile | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 11/12 | 1340/1693 | 1158/1323 | 386/440 | chr1 | 44725165 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44674854
|
C | T | 1 | a0001c0001t0002 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/12 | chr1 | 44674854 | ||||||
| chr1:44725507
|
G | A | 1 | a0001c0001t0003 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 12/12 | 104 | chr1 | 44725507 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44674904
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+31C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44674904 | ||||||
| chr1:44674935
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-23+62T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44674935 | ||||||
| chr1:44674947
|
C | CTGGA | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 28 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+102_-23+105dup others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44674947 | |||||
| chr1:44674947
|
C | CTGGATGG others(5): Show |
1 | a0001c0001t0001g0015 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-23+94_-23+105dupA others(11): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44674947 | |||||
| chr1:44674947
|
C | CTGGATGG others(9): Show |
1 | a0001c0001t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-23+90_-23+105dupA others(15): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44674947 | |||||
| chr1:44674947
|
CTGGA | C | 91 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0184others(88): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-23+102_-23+105del others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44674947 | |||||
| chr1:44674961
|
GGAT | G | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+90_-23+92delAT others(1): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44674961 | |||||
| chr1:44675165
|
A | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23+292A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44675165 | ||||||
| chr1:44675833
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-23+960A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44675833 | ||||||
| chr1:44675949
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0184a0001c0001t0001g0185others(35): Show | 39 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-23+1076G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44675949 | ||||||
| chr1:44675973
|
C | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-23+1100C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44675973 | ||||||
| chr1:44676074
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-23+1201T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676074 | ||||||
| chr1:44676114
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23+1241A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676114 | ||||||
| chr1:44676334
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0183 | 3 | HG00639.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+1461G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676334 | ||||||
| chr1:44676367
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00408.hp2 HG00438.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+1494G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676367 | ||||||
| chr1:44676399
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-23+1526C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676399 | ||||||
| chr1:44676404
|
A | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(23): Show | 27 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+1531A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676404 | ||||||
| chr1:44676485
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-23+1612G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676485 | ||||||
| chr1:44676537
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-23+1664A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676537 | ||||||
| chr1:44676623
|
T | G | 68 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(65): Show | 70 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.-23+1750T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676623 | ||||||
| chr1:44676666
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-23+1793T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676666 | ||||||
| chr1:44676744
|
G | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+1871G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676744 | ||||||
| chr1:44676800
|
G | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(23): Show | 27 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+1927G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676800 | ||||||
| chr1:44677271
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG00099.hp2 HG02698.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+2398G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677271 | ||||||
| chr1:44677388
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0222a0001c0001t0002g0223 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+2515G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677388 | ||||||
| chr1:44677402
|
G | C | 7 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(4): Show | 7 | HG02559.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+2529G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677402 | ||||||
| chr1:44677484
|
GA | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(23): Show | 27 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+2619delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44677484 | |||||
| chr1:44677502
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0017 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-23+2629T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677502 | ||||||
| chr1:44677519
|
T | A | 16 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(13): Show | 16 | HG00642.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+2646T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677519 | ||||||
| chr1:44677669
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-23+2796C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677669 | ||||||
| chr1:44677743
|
C | G | 68 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(65): Show | 70 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.-23+2870C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677743 | ||||||
| chr1:44677800
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-23+2927A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44677800 | ||||||
| chr1:44678288
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-23+3415G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678288 | ||||||
| chr1:44678354
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+3481G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678354 | ||||||
| chr1:44678413
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 6 | HG01261.hp2 HG01358.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+3540G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678413 | ||||||
| chr1:44678630
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 28 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+3757C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678630 | ||||||
| chr1:44678794
|
CG | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 28 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+3928delG | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44678794 | |||||
| chr1:44678907
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-23+4034G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678907 | ||||||
| chr1:44678962
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-23+4089T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44678962 | ||||||
| chr1:44679135
|
G | A | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02809.hp1 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+4262G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679135 | ||||||
| chr1:44679178
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(125): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-23+4305T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679178 | ||||||
| chr1:44679184
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(125): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-23+4311G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679184 | ||||||
| chr1:44679235
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-23+4362G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679235 | ||||||
| chr1:44679632
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0185a0001c0001t0001g0186 | 4 | HG02083.hp1 HG02738.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+4759G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679632 | ||||||
| chr1:44679645
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-23+4772C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679645 | ||||||
| chr1:44679650
|
T | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0184a0001c0001t0001g0185others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-23+4777T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679650 | ||||||
| chr1:44679848
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-23+4975G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679848 | ||||||
| chr1:44680166
|
A | AGTTT | 5 | a0001c0001t0001g0047a0001c0001t0001g0180a0001c0001t0001g0219others(2): Show | 5 | HG02056.hp2 HG03225.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+5321_-23+5324d others(6): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44680166 | |||||
| chr1:44680166
|
AGTTT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(33): Show | 38 | HG00280.hp2 HG01123.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-23+5321_-23+5324d others(6): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44680166 | |||||
| chr1:44680321
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+5448C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680321 | ||||||
| chr1:44680465
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-23+5592C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680465 | ||||||
| chr1:44680485
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-23+5612T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680485 | ||||||
| chr1:44680591
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0055 | 3 | HG01993.hp2 HG02273.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-23+5718G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680591 | ||||||
| chr1:44680600
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0017 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-23+5727A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680600 | ||||||
| chr1:44680736
|
C | T | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 99 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-23+5863C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680736 | ||||||
| chr1:44680761
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-23+5888C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680761 | ||||||
| chr1:44680761
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 45 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23+5888C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680761 | ||||||
| chr1:44680915
|
TATC | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+6047_-23+6049d others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44680915 | |||||
| chr1:44680976
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0184a0001c0001t0001g0185others(38): Show | 43 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-23+6103A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44680976 | ||||||
| chr1:44680996
|
C | CT | 29 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(26): Show | 30 | HG00639.hp1 HG00642.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+6139dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44680996 | |||||
| chr1:44681063
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 102 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-23+6190C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681063 | ||||||
| chr1:44681090
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+6217G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681090 | ||||||
| chr1:44681134
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0224others(40): Show | 44 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-23+6261G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681134 | ||||||
| chr1:44681151
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-23+6278T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681151 | ||||||
| chr1:44681198
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-23+6325T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681198 | ||||||
| chr1:44681247
|
A | G | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-23+6374A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681247 | ||||||
| chr1:44681265
|
G | C | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-23+6392G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681265 | ||||||
| chr1:44681575
|
AG | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 28 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+6704delG | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44681575 | |||||
| chr1:44681582
|
A | C | 50 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(47): Show | 52 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.-23+6709A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681582 | ||||||
| chr1:44681613
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-23+6740G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681613 | ||||||
| chr1:44681823
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-23+6950G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44681823 | ||||||
| chr1:44682011
|
C | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+7138C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682011 | ||||||
| chr1:44682082
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-23+7209C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682082 | ||||||
| chr1:44682215
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02451.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-23+7342A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682215 | ||||||
| chr1:44682327
|
T | C | 2 | a0001c0001t0001g0017a0002c0003t0001g0274 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-22-7349T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682327 | ||||||
| chr1:44682624
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-7052T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682624 | ||||||
| chr1:44682868
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 7 | HG01123.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-6808C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682868 | ||||||
| chr1:44682899
|
C | T | 2 | a0001c0001t0001g0265a0003c0002t0001g0264 | 2 | HG01167.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-22-6777C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44682899 | ||||||
| chr1:44683004
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-22-6672G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683004 | ||||||
| chr1:44683196
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-22-6480G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683196 | ||||||
| chr1:44683268
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-22-6408G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683268 | ||||||
| chr1:44683444
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-22-6232A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683444 | ||||||
| chr1:44683676
|
T | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0222a0001c0001t0002g0223 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-6000T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683676 | ||||||
| chr1:44683765
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 36 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-22-5911C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683765 | ||||||
| chr1:44683987
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0062 | 3 | NA18943.hp1 NA18957.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-22-5689T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44683987 | ||||||
| chr1:44684005
|
C | CAG | 40 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(37): Show | 41 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.-22-5656_-22-5655d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44684005 | |||||
| chr1:44684044
|
G | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-22-5632G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684044 | ||||||
| chr1:44684141
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-22-5535T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684141 | ||||||
| chr1:44684153
|
G | C | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-5523G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684153 | ||||||
| chr1:44684251
|
A | T | 1 | a0001c0001t0001g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-22-5425A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684251 | ||||||
| chr1:44684548
|
C | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-5128C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684548 | ||||||
| chr1:44684711
|
T | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-4965T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44684711 | ||||||
| chr1:44685041
|
G | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-4635G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685041 | ||||||
| chr1:44685159
|
T | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-4517T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685159 | ||||||
| chr1:44685160
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-22-4516A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685160 | ||||||
| chr1:44685278
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-4398T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685278 | ||||||
| chr1:44685312
|
C | CT | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0170others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-4351dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44685312 | |||||
| chr1:44685336
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-22-4340T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685336 | ||||||
| chr1:44685343
|
G | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-4333G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685343 | ||||||
| chr1:44685354
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0222a0001c0001t0002g0223 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4322G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685354 | ||||||
| chr1:44685393
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-22-4283C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685393 | ||||||
| chr1:44685525
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18953.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-22-4151G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685525 | ||||||
| chr1:44685634
|
C | CT | 44 | a0001c0001t0001g0010a0001c0001t0001g0039a0001c0001t0001g0184others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-22-4030dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44685634 | |||||
| chr1:44685722
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-22-3954G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685722 | ||||||
| chr1:44685773
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(37): Show | 41 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.-22-3903A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685773 | ||||||
| chr1:44685774
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-22-3902C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685774 | ||||||
| chr1:44685861
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-3815C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44685861 | ||||||
| chr1:44686067
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG00099.hp2 HG02698.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-3609G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44686067 | ||||||
| chr1:44686080
|
G | A | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-3596G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44686080 | ||||||
| chr1:44686606
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-22-3070G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44686606 | ||||||
| chr1:44686619
|
T | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0184a0001c0001t0001g0185others(34): Show | 38 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-22-3057T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44686619 | ||||||
| chr1:44686875
|
A | C | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-2801A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44686875 | ||||||
| chr1:44686953
|
GA | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0017others(10): Show | 13 | HG02622.hp2 HG02896.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-2706delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 44686953 | |||||
| chr1:44687315
|
A | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0180a0004c0005t0001g0168 | 3 | HG00621.hp1 HG02056.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-22-2361A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687315 | ||||||
| chr1:44687317
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-2359A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687317 | ||||||
| chr1:44687374
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-22-2302G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687374 | ||||||
| chr1:44687444
|
T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 28 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22-2232T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687444 | ||||||
| chr1:44687459
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22-2217G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687459 | ||||||
| chr1:44687505
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-2171G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687505 | ||||||
| chr1:44687602
|
G | A | 5 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-2074G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687602 | ||||||
| chr1:44687604
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-22-2072C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687604 | ||||||
| chr1:44687709
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1967G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687709 | ||||||
| chr1:44687861
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-22-1815G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687861 | ||||||
| chr1:44687898
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-1778C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687898 | ||||||
| chr1:44687917
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-1759G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687917 | ||||||
| chr1:44687938
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-1738G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44687938 | ||||||
| chr1:44688005
|
G | C | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-1671G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688005 | ||||||
| chr1:44688285
|
A | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-22-1391A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688285 | ||||||
| chr1:44688290
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-1386G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688290 | ||||||
| chr1:44688494
|
T | C | 5 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-1182T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688494 | ||||||
| chr1:44688732
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00438.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-944A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688732 | ||||||
| chr1:44688779
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02165.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-22-897A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688779 | ||||||
| chr1:44688866
|
A | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-810A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688866 | ||||||
| chr1:44688868
|
T | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0222a0001c0001t0002g0223 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-808T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688868 | ||||||
| chr1:44688890
|
T | A | 44 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0183others(41): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-22-786T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688890 | ||||||
| chr1:44688918
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-22-758G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688918 | ||||||
| chr1:44688953
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-723G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44688953 | ||||||
| chr1:44689058
|
TC | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-617delC | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689058 | ||||||
| chr1:44689102
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-22-574C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689102 | ||||||
| chr1:44689125
|
G | A | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-551G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689125 | ||||||
| chr1:44689126
|
C | T | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-22-550C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689126 | ||||||
| chr1:44689132
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-544C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689132 | ||||||
| chr1:44689153
|
C | T | 1 | a0001c0001t0001g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-22-523C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689153 | ||||||
| chr1:44689164
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-512G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689164 | ||||||
| chr1:44689179
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-22-497C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689179 | ||||||
| chr1:44689225
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-451G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689225 | ||||||
| chr1:44689254
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-22-422G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689254 | ||||||
| chr1:44689259
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-22-417C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689259 | ||||||
| chr1:44689328
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-348G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689328 | ||||||
| chr1:44689358
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-318C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689358 | ||||||
| chr1:44689365
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-311G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689365 | ||||||
| chr1:44689442
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-234T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689442 | ||||||
| chr1:44689549
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0002g0011a0001c0001t0002g0222others(1): Show | 5 | HG01069.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-127T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689549 | ||||||
| chr1:44689554
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-122G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44689554 | ||||||
| chr1:44689987
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.206+84A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44689987 | ||||||
| chr1:44690207
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.206+304G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690207 | ||||||
| chr1:44690282
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+379G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690282 | ||||||
| chr1:44690328
|
T | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+425T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690328 | ||||||
| chr1:44690341
|
TA | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+448delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44690341 | |||||
| chr1:44690397
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.206+494T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690397 | ||||||
| chr1:44690503
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+600T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690503 | ||||||
| chr1:44690800
|
T | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02622.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.206+897T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690800 | ||||||
| chr1:44690925
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.206+1022G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690925 | ||||||
| chr1:44690980
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+1077C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44690980 | ||||||
| chr1:44691061
|
A | AC | 42 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 44 | HG00280.hp2 HG01069.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.206+1159dupC | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44691061 | |||||
| chr1:44691230
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(22): Show | 26 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.206+1327C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691230 | ||||||
| chr1:44691281
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.206+1378A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691281 | ||||||
| chr1:44691468
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+1565C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691468 | ||||||
| chr1:44691735
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.206+1832C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691735 | ||||||
| chr1:44691736
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+1833A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691736 | ||||||
| chr1:44691737
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+1834_206+1835i others(13): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691737 | ||||||
| chr1:44691738
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+1835C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691738 | ||||||
| chr1:44691770
|
T | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+1867T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691770 | ||||||
| chr1:44691773
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.206+1870G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691773 | ||||||
| chr1:44691943
|
A | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+2040A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44691943 | ||||||
| chr1:44692031
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+2128A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692031 | ||||||
| chr1:44692041
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+2138C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692041 | ||||||
| chr1:44692066
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(22): Show | 26 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.206+2163T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692066 | ||||||
| chr1:44692231
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.206+2328G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692231 | ||||||
| chr1:44692340
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.206+2437G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692340 | ||||||
| chr1:44692425
|
ATTG | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0071 | 3 | HG02970.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.206+2525_206+2527d others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44692425 | |||||
| chr1:44692567
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.206+2664A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692567 | ||||||
| chr1:44692614
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.206+2711C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692614 | ||||||
| chr1:44692875
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+2972T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692875 | ||||||
| chr1:44692881
|
T | C | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.206+2978T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692881 | ||||||
| chr1:44692956
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+3053T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44692956 | ||||||
| chr1:44693202
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.206+3299C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44693202 | ||||||
| chr1:44693461
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+3558C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44693461 | ||||||
| chr1:44693537
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0224others(14): Show | 18 | HG00639.hp1 HG00642.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.207-3565C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44693537 | ||||||
| chr1:44693576
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019 | 4 | HG01261.hp2 HG01358.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-3526G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44693576 | ||||||
| chr1:44693730
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207-3372A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44693730 | ||||||
| chr1:44694227
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.207-2875G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694227 | ||||||
| chr1:44694408
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.207-2694C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694408 | ||||||
| chr1:44694509
|
CT | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 79 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.207-2575delT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44694509 | |||||
| chr1:44694509
|
CTT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.207-2576_207-2575d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44694509 | |||||
| chr1:44694619
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.207-2483C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694619 | ||||||
| chr1:44694629
|
C | T | 6 | a0001c0001t0001g0229a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-2473C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694629 | ||||||
| chr1:44694778
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.207-2324A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694778 | ||||||
| chr1:44694873
|
T | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(3): Show | 6 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-2229T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44694873 | ||||||
| chr1:44695003
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.207-2099C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695003 | ||||||
| chr1:44695437
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207-1665T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695437 | ||||||
| chr1:44695481
|
T | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-1621T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695481 | ||||||
| chr1:44695496
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-1606A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695496 | ||||||
| chr1:44695544
|
TA | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(128): Show | 135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.207-1555delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44695544 | |||||
| chr1:44695582
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0221others(3): Show | 6 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-1520A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695582 | ||||||
| chr1:44695743
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 52 | HG00280.hp2 HG01069.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.207-1359T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695743 | ||||||
| chr1:44695766
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.207-1336C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695766 | ||||||
| chr1:44695879
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18948.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.207-1223A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695879 | ||||||
| chr1:44695881
|
C | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(128): Show | 135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.207-1221C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695881 | ||||||
| chr1:44695944
|
CA | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.207-1141delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44695944 | |||||
| chr1:44695986
|
G | C | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG02451.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.207-1116G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695986 | ||||||
| chr1:44696025
|
G | GA | 27 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 28 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.207-1072dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 44696025 | |||||
| chr1:44696033
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.207-1069G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44696033 | ||||||
| chr1:44696089
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-1013A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44696089 | ||||||
| chr1:44696173
|
C | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.207-929C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44696173 | ||||||
| chr1:44696230
|
A | G | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0024others(57): Show | 62 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.207-872A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44696230 | ||||||
| chr1:44696531
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.207-571C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44696531 | ||||||
| chr1:44697211
|
A | G | 1 | a0002c0003t0001g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+41A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697211 | ||||||
| chr1:44697272
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275+102G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697272 | ||||||
| chr1:44697355
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.275+185T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697355 | ||||||
| chr1:44697598
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.275+428A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697598 | ||||||
| chr1:44697683
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.276-380T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697683 | ||||||
| chr1:44697690
|
AATTTAGG others(4): Show |
A | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02738.hp1 HG03017.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-370_276-360del others(11): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 44697690 | |||||
| chr1:44697759
|
T | TCACCC | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | HG02738.hp1 HG03017.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-299_276-295dup others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 44697759 | |||||
| chr1:44697880
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.276-183G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697880 | ||||||
| chr1:44697975
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(29): Show | 33 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.276-88A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 3/11 | chr1 | 44697975 | ||||||
| chr1:44698405
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.442+176T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698405 | ||||||
| chr1:44698495
|
G | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+266G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698495 | ||||||
| chr1:44698503
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.442+274A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698503 | ||||||
| chr1:44698532
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.442+303C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698532 | ||||||
| chr1:44698568
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.442+339T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698568 | ||||||
| chr1:44698813
|
C | CA | 37 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(34): Show | 39 | HG00280.hp2 HG01069.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.442+598dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44698813 | |||||
| chr1:44698813
|
CA | C | 31 | a0001c0001t0001g0066a0001c0001t0001g0108a0001c0001t0001g0161others(28): Show | 31 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.442+598delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44698813 | |||||
| chr1:44698827
|
A | C | 1 | a0001c0004t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.442+598A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698827 | ||||||
| chr1:44698879
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.442+650G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44698879 | ||||||
| chr1:44699279
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442+1050G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699279 | ||||||
| chr1:44699283
|
C | CA | 14 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(11): Show | 14 | HG00621.hp2 HG02074.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.442+1074dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699283 | |||||
| chr1:44699283
|
C | CAA | 19 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(16): Show | 20 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.442+1073_442+1074d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699283 | |||||
| chr1:44699283
|
CA | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0070others(4): Show | 7 | HG01243.hp1 HG02015.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1074delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699283 | |||||
| chr1:44699302
|
A | AT | 3 | a0001c0001t0002g0011a0001c0001t0002g0222a0001c0001t0002g0223 | 4 | HG01069.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1073_442+1074i others(3): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699302 | ||||||
| chr1:44699443
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.442+1214T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699443 | ||||||
| chr1:44699472
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.442+1243C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699472 | ||||||
| chr1:44699505
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.442+1276G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699505 | ||||||
| chr1:44699647
|
C | T | 29 | a0001c0001t0001g0066a0001c0001t0001g0156a0001c0001t0001g0161others(26): Show | 29 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.443-1276C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699647 | ||||||
| chr1:44699689
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0001g0148others(1): Show | 5 | HG02630.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-1234C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699689 | ||||||
| chr1:44699742
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 72 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.443-1181G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699742 | ||||||
| chr1:44699832
|
A | AT | 13 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 15 | HG01069.hp2 HG01261.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.443-1076dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699832 | |||||
| chr1:44699832
|
AT | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02809.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-1076delT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699832 | |||||
| chr1:44699861
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG02071.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.443-1062G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699861 | ||||||
| chr1:44699951
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0201others(9): Show | 13 | HG00639.hp1 HG00642.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.443-972T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44699951 | ||||||
| chr1:44699994
|
T | TAATTTTT others(331): Show |
1 | a0001c0001t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.443-914_443-913ins others(338): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44699994 | |||||
| chr1:44700002
|
G | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02809.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-921G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700002 | ||||||
| chr1:44700066
|
G | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0070a0001c0001t0001g0076others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-857G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700066 | ||||||
| chr1:44700153
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.443-770T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700153 | ||||||
| chr1:44700235
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.443-688C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700235 | ||||||
| chr1:44700344
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.443-579G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700344 | ||||||
| chr1:44700360
|
C | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0106a0001c0001t0001g0207 | 3 | HG00408.hp1 NA19005.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.443-563C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700360 | ||||||
| chr1:44700413
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.443-510A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700413 | ||||||
| chr1:44700414
|
A | G | 36 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0017others(33): Show | 37 | HG00639.hp1 HG00642.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.443-509A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700414 | ||||||
| chr1:44700417
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.443-506A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700417 | ||||||
| chr1:44700440
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.443-483A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700440 | ||||||
| chr1:44700444
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.443-479T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700444 | ||||||
| chr1:44700490
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.443-433C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700490 | ||||||
| chr1:44700571
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG02145.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-352G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700571 | ||||||
| chr1:44700615
|
CA | C | 58 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(55): Show | 59 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.443-289delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 44700615 | |||||
| chr1:44700711
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0036others(40): Show | 44 | HG00099.hp1 HG00408.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.443-212T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700711 | ||||||
| chr1:44700824
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.443-99G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700824 | ||||||
| chr1:44700841
|
T | A | 141 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(138): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.443-82T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 4/11 | chr1 | 44700841 | ||||||
| chr1:44701213
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.639+94C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44701213 | ||||||
| chr1:44701471
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.639+352G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44701471 | ||||||
| chr1:44701492
|
C | CT | 27 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(24): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.639+385dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44701492 | |||||
| chr1:44701757
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.639+638T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44701757 | ||||||
| chr1:44701923
|
CA | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(46): Show | 53 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.639+817delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44701923 | |||||
| chr1:44702323
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0195 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.639+1204C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702323 | ||||||
| chr1:44702338
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.639+1219A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702338 | ||||||
| chr1:44702429
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.639+1310C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702429 | ||||||
| chr1:44702439
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.639+1320C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702439 | ||||||
| chr1:44702477
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.639+1358G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702477 | ||||||
| chr1:44702572
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.639+1453C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702572 | ||||||
| chr1:44702573
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.639+1454G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702573 | ||||||
| chr1:44702710
|
C | CA | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.640-1361dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44702710 | |||||
| chr1:44702710
|
C | CAA | 18 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0036others(15): Show | 18 | HG00438.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.640-1362_640-1361d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44702710 | |||||
| chr1:44702808
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.640-1281C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702808 | ||||||
| chr1:44702989
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0229a0001c0001t0001g0269others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-1100G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44702989 | ||||||
| chr1:44703054
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(47): Show | 51 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.640-1035T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703054 | ||||||
| chr1:44703109
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0221a0001c0001t0001g0229others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.640-980A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703109 | ||||||
| chr1:44703138
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 167 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.640-951G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703138 | ||||||
| chr1:44703190
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.640-899T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703190 | ||||||
| chr1:44703214
|
C | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0229a0001c0001t0001g0269others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-875C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703214 | ||||||
| chr1:44703338
|
C | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02809.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-751C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703338 | ||||||
| chr1:44703361
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640-728C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703361 | ||||||
| chr1:44703515
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640-574G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703515 | ||||||
| chr1:44703548
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 37 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.640-541C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703548 | ||||||
| chr1:44703560
|
T | TAAA | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 53 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.640-512_640-510dup others(3): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44703560 | |||||
| chr1:44703560
|
T | TAAAA | 86 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(83): Show | 88 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.640-513_640-510dup others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44703560 | |||||
| chr1:44703560
|
T | TAAAAA | 9 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0042others(6): Show | 9 | HG00438.hp1 HG02109.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.640-514_640-510dup others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 44703560 | |||||
| chr1:44703561
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640-528A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703561 | ||||||
| chr1:44703713
|
G | T | 1 | a0003c0002t0001g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.640-376G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703713 | ||||||
| chr1:44703717
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.640-372G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703717 | ||||||
| chr1:44703845
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.640-244G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703845 | ||||||
| chr1:44703964
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0193 | 2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.640-125G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703964 | ||||||
| chr1:44703965
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.640-124A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 5/11 | chr1 | 44703965 | ||||||
| chr1:44704253
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724+80G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704253 | ||||||
| chr1:44704340
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 169 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.724+167A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704340 | ||||||
| chr1:44704372
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+199C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704372 | ||||||
| chr1:44704489
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0258 | 3 | HG00099.hp1 HG00735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.724+316G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704489 | ||||||
| chr1:44704506
|
G | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+333G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704506 | ||||||
| chr1:44704517
|
G | GT | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.724+356dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44704517 | |||||
| chr1:44704517
|
G | GTT | 8 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0065others(5): Show | 8 | HG02129.hp2 HG02280.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+355_724+356dup others(2): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44704517 | |||||
| chr1:44704713
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0201others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+540T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704713 | ||||||
| chr1:44704787
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.724+614C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704787 | ||||||
| chr1:44704834
|
C | CT | 34 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0040others(31): Show | 35 | HG00099.hp2 HG00408.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.724+679dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44704834 | |||||
| chr1:44704834
|
CT | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0195others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.724+679delT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44704834 | |||||
| chr1:44704869
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+696C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704869 | ||||||
| chr1:44704896
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+723G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704896 | ||||||
| chr1:44704974
|
A | G | 2 | a0003c0002t0001g0136a0003c0002t0001g0264 | 2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.724+801A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44704974 | ||||||
| chr1:44705026
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.724+853G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705026 | ||||||
| chr1:44705070
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 155 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.724+897C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705070 | ||||||
| chr1:44705152
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+979T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705152 | ||||||
| chr1:44705229
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.724+1056G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705229 | ||||||
| chr1:44705238
|
T | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 37 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.724+1065T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705238 | ||||||
| chr1:44705318
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.724+1145C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705318 | ||||||
| chr1:44705320
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+1147G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705320 | ||||||
| chr1:44705573
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.724+1400A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705573 | ||||||
| chr1:44705907
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.724+1734G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705907 | ||||||
| chr1:44705970
|
T | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+1797T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44705970 | ||||||
| chr1:44706025
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+1852G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706025 | ||||||
| chr1:44706356
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.724+2183G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706356 | ||||||
| chr1:44706484
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.724+2311G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706484 | ||||||
| chr1:44706504
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.724+2331C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706504 | ||||||
| chr1:44706585
|
T | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0040others(24): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.724+2412T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706585 | ||||||
| chr1:44706632
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+2459C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706632 | ||||||
| chr1:44706818
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.724+2645C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706818 | ||||||
| chr1:44706973
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.724+2800C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706973 | ||||||
| chr1:44706980
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0001t0001g0212 | 3 | NA18948.hp1 NA19054.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.724+2807C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44706980 | ||||||
| chr1:44707247
|
C | CTGAGTGA others(1): Show |
5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02809.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+3096_724+3103d others(10): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44707247 | |||||
| chr1:44707247
|
CTGAG | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0229a0001c0001t0001g0269others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+3100_724+3103d others(6): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44707247 | |||||
| chr1:44707422
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.724+3249T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44707422 | ||||||
| chr1:44707579
|
C | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+3406C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44707579 | ||||||
| chr1:44707679
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 177 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.724+3506T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44707679 | ||||||
| chr1:44707695
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.724+3522C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44707695 | ||||||
| chr1:44708088
|
A | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0108others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.724+3915A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708088 | ||||||
| chr1:44708183
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.724+4010A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708183 | ||||||
| chr1:44708214
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.724+4041T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708214 | ||||||
| chr1:44708219
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0229a0001c0001t0001g0269others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+4046G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708219 | ||||||
| chr1:44708604
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724+4431G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708604 | ||||||
| chr1:44708641
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.724+4468C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708641 | ||||||
| chr1:44708642
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.724+4469G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708642 | ||||||
| chr1:44708729
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.724+4556A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44708729 | ||||||
| chr1:44709006
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG01123.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.724+4833A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709006 | ||||||
| chr1:44709153
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.724+4980C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709153 | ||||||
| chr1:44709317
|
C | CT | 8 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0201others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.724+5145dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44709317 | |||||
| chr1:44709338
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.724+5165T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709338 | ||||||
| chr1:44709398
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.724+5225C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709398 | ||||||
| chr1:44709400
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0162others(10): Show | 13 | HG00642.hp1 HG01952.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+5227C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709400 | ||||||
| chr1:44709410
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(216): Show | 226 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.724+5237C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709410 | ||||||
| chr1:44709411
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724+5238G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709411 | ||||||
| chr1:44709415
|
T | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0019others(32): Show | 37 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.724+5242T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709415 | ||||||
| chr1:44709422
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724+5249C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709422 | ||||||
| chr1:44709423
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724+5250A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709423 | ||||||
| chr1:44709439
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.724+5266A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709439 | ||||||
| chr1:44709443
|
G | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01361.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.724+5270G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709443 | ||||||
| chr1:44709443
|
G | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(19): Show | 23 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.724+5270G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709443 | ||||||
| chr1:44709444
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.724+5271G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709444 | ||||||
| chr1:44709446
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724+5273G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709446 | ||||||
| chr1:44709447
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.724+5274C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709447 | ||||||
| chr1:44709448
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0036others(18): Show | 22 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.724+5275G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709448 | ||||||
| chr1:44709455
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.724+5282G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709455 | ||||||
| chr1:44709468
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0217 | 2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.724+5295C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709468 | ||||||
| chr1:44709468
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.724+5295C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709468 | ||||||
| chr1:44709472
|
A | G | 2 | a0001c0001t0001g0221a0001c0004t0001g0111 | 2 | HG00738.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.724+5299A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709472 | ||||||
| chr1:44709476
|
T | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0217 | 2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.724+5303T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709476 | ||||||
| chr1:44709483
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0121a0001c0001t0001g0217 | 3 | HG00438.hp2 HG00738.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.724+5310T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709483 | ||||||
| chr1:44709489
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0104a0001c0001t0001g0179 | 3 | HG02056.hp1 NA18966.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.724+5316G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709489 | ||||||
| chr1:44709495
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.724+5322A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709495 | ||||||
| chr1:44709496
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.724+5323C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709496 | ||||||
| chr1:44709500
|
A | G | 14 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0071others(11): Show | 14 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.724+5327A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709500 | ||||||
| chr1:44709541
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0257a0001c0001t0001g0263others(1): Show | 4 | HG01516.hp1 HG02683.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+5368A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709541 | ||||||
| chr1:44709542
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.724+5369T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709542 | ||||||
| chr1:44709542
|
T | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0097a0001c0001t0001g0139others(5): Show | 8 | HG01516.hp1 HG02683.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+5369T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709542 | ||||||
| chr1:44709543
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.724+5370G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709543 | ||||||
| chr1:44709549
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.724+5376G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709549 | ||||||
| chr1:44709552
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0148a0001c0001t0001g0240 | 4 | HG02630.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+5379G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709552 | ||||||
| chr1:44709558
|
C | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | HG01516.hp1 HG01993.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+5385C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709558 | ||||||
| chr1:44709574
|
AG | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0183 | 3 | HG00639.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.724+5403delG | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44709574 | |||||
| chr1:44709672
|
GA | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 45 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.724+5514delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44709672 | |||||
| chr1:44709706
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02615.hp1 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.724+5533G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709706 | ||||||
| chr1:44709717
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.724+5544G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709717 | ||||||
| chr1:44709726
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.724+5553A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709726 | ||||||
| chr1:44709854
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.724+5681A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709854 | ||||||
| chr1:44709940
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0201 | 3 | HG01243.hp1 HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.724+5767C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709940 | ||||||
| chr1:44710017
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.724+5844G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710017 | ||||||
| chr1:44710083
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0236 | 3 | HG02559.hp1 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.724+5910G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710083 | ||||||
| chr1:44710112
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0193 | 2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.724+5939G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710112 | ||||||
| chr1:44710149
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.724+5976C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710149 | ||||||
| chr1:44710253
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.724+6080G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710253 | ||||||
| chr1:44710406
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.724+6233G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710406 | ||||||
| chr1:44710466
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.724+6293G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710466 | ||||||
| chr1:44710502
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.724+6329G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710502 | ||||||
| chr1:44710515
|
A | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0060a0001c0001t0001g0092others(5): Show | 8 | HG00280.hp2 NA18979.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+6342A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710515 | ||||||
| chr1:44710566
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.724+6393G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710566 | ||||||
| chr1:44710603
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.724+6430C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710603 | ||||||
| chr1:44710608
|
CA | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.724+6456delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44710608 | |||||
| chr1:44710608
|
CAA | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.724+6455_724+6456d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44710608 | |||||
| chr1:44710613
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0094 | 3 | HG03491.hp1 HG03492.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.724+6440A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710613 | ||||||
| chr1:44710625
|
A | G | 1 | a0001c0001t0003g0218 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+6452A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710625 | ||||||
| chr1:44710720
|
C | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG00099.hp1 HG00735.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+6547C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710720 | ||||||
| chr1:44710810
|
C | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0275 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.724+6637C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710810 | ||||||
| chr1:44710837
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.724+6664C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710837 | ||||||
| chr1:44710969
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.724+6796T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44710969 | ||||||
| chr1:44711198
|
G | T | 1 | a0001c0001t0001g0013 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.724+7025G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44711198 | ||||||
| chr1:44711399
|
G | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG00099.hp2 HG01516.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+7226G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44711399 | ||||||
| chr1:44711647
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.724+7474A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44711647 | ||||||
| chr1:44712064
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.724+7891C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712064 | ||||||
| chr1:44712143
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.724+7970G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712143 | ||||||
| chr1:44712209
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.724+8036A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712209 | ||||||
| chr1:44712275
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.724+8102A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712275 | ||||||
| chr1:44712535
|
C | CA | 34 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0041others(31): Show | 34 | HG00438.hp2 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.724+8384dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44712535 | |||||
| chr1:44712535
|
CA | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 99 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.724+8384delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44712535 | |||||
| chr1:44712740
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 40 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.724+8567T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712740 | ||||||
| chr1:44712802
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724+8629T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44712802 | ||||||
| chr1:44713034
|
T | TAAGACGG others(36): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0133 | 2 | NA18994.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.724+8866_724+8908d others(45): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44713034 | |||||
| chr1:44713097
|
C | CT | 42 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 42 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.724+8945dupT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44713097 | |||||
| chr1:44713097
|
CT | C | 44 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0025others(41): Show | 44 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.724+8945delT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44713097 | |||||
| chr1:44713097
|
CTTT | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0083others(7): Show | 11 | HG01123.hp1 HG02080.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.724+8943_724+8945d others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44713097 | |||||
| chr1:44713098
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.724+8925T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44713098 | ||||||
| chr1:44713262
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.724+9089C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44713262 | ||||||
| chr1:44714087
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0229a0001c0001t0001g0269others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+9914T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714087 | ||||||
| chr1:44714219
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.725-9903G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714219 | ||||||
| chr1:44714256
|
C | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0025others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.725-9866C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714256 | ||||||
| chr1:44714278
|
G | GA | 11 | a0001c0001t0001g0096a0001c0001t0001g0125a0001c0001t0001g0144others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(8): Show |
intron_variant | MODIFIER | c.725-9830dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44714278 | |||||
| chr1:44714453
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.725-9669T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714453 | ||||||
| chr1:44714585
|
C | CA | 20 | a0001c0001t0001g0024a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG00408.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.725-9522dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44714585 | |||||
| chr1:44714685
|
T | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0067a0001c0001t0001g0068others(13): Show | 16 | HG00642.hp1 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.725-9437T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714685 | ||||||
| chr1:44714822
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.725-9300T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714822 | ||||||
| chr1:44714867
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02258.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.725-9255T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714867 | ||||||
| chr1:44714901
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0162 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.725-9221G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44714901 | ||||||
| chr1:44715144
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.725-8978T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715144 | ||||||
| chr1:44715224
|
G | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 40 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.725-8898G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715224 | ||||||
| chr1:44715230
|
T | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0083others(8): Show | 12 | HG01123.hp1 HG02080.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.725-8892T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715230 | ||||||
| chr1:44715472
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.725-8650C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715472 | ||||||
| chr1:44715635
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.725-8487A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715635 | ||||||
| chr1:44715640
|
A | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-8482A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715640 | ||||||
| chr1:44715691
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.725-8431C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715691 | ||||||
| chr1:44715869
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.725-8253G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715869 | ||||||
| chr1:44715939
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.725-8183G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44715939 | ||||||
| chr1:44716145
|
AT | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(75): Show | 79 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.725-7966delT | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44716145 | |||||
| chr1:44716939
|
T | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-7183T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44716939 | ||||||
| chr1:44717145
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.725-6977G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717145 | ||||||
| chr1:44717219
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.725-6903T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717219 | ||||||
| chr1:44717306
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.725-6816A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717306 | ||||||
| chr1:44717522
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.725-6600A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717522 | ||||||
| chr1:44717857
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.725-6265C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717857 | ||||||
| chr1:44717858
|
G | A | 7 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0108others(4): Show | 7 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-6264G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44717858 | ||||||
| chr1:44718454
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0001g0211 | 3 | NA18948.hp2 NA18979.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.725-5668C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718454 | ||||||
| chr1:44718587
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.725-5535A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718587 | ||||||
| chr1:44718634
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(79): Show | 84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.725-5488C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718634 | ||||||
| chr1:44718639
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.725-5483G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718639 | ||||||
| chr1:44718790
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.725-5332C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718790 | ||||||
| chr1:44718797
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0180 | 2 | HG02056.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.725-5325G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718797 | ||||||
| chr1:44718835
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.725-5287A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44718835 | ||||||
| chr1:44719025
|
G | GA | 23 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0058others(20): Show | 23 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.725-5075dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44719025 | |||||
| chr1:44719025
|
G | GAA | 90 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(87): Show | 93 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.725-5076_725-5075d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44719025 | |||||
| chr1:44719025
|
G | GAAA | 8 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0148others(5): Show | 9 | HG02055.hp2 HG02074.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.725-5077_725-5075d others(5): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44719025 | |||||
| chr1:44719025
|
G | GGA | 5 | a0001c0001t0001g0042a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-5097_725-5096i others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719025 | ||||||
| chr1:44719026
|
A | G | 1 | a0001c0001t0002g0011 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.725-5096A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719026 | ||||||
| chr1:44719242
|
T | TG | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.725-4880_725-4879i others(3): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719242 | ||||||
| chr1:44719342
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.725-4780G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719342 | ||||||
| chr1:44719589
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.725-4533A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719589 | ||||||
| chr1:44719707
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.725-4415C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44719707 | ||||||
| chr1:44720005
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.725-4117G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720005 | ||||||
| chr1:44720136
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0148a0001c0001t0001g0240 | 4 | HG02630.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-3986G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720136 | ||||||
| chr1:44720197
|
C | CA | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 86 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.725-3902dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44720197 | |||||
| chr1:44720197
|
C | CAA | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(27): Show | 32 | HG00621.hp2 HG00735.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.725-3903_725-3902d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44720197 | |||||
| chr1:44720197
|
CA | C | 10 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0062others(7): Show | 10 | HG01168.hp2 HG01975.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-3902delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44720197 | |||||
| chr1:44720197
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.725-3911_725-3902d others(12): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44720197 | |||||
| chr1:44720238
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.725-3884C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720238 | ||||||
| chr1:44720384
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 110 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.725-3738G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720384 | ||||||
| chr1:44720573
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.725-3549A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720573 | ||||||
| chr1:44720769
|
C | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0118others(7): Show | 10 | HG00639.hp2 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.725-3353C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720769 | ||||||
| chr1:44720895
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.725-3227G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44720895 | ||||||
| chr1:44721076
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | NA18942.hp2 NA19004.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.725-3046G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721076 | ||||||
| chr1:44721452
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.725-2670A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721452 | ||||||
| chr1:44721513
|
T | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(6): Show | 9 | HG02630.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.725-2609T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721513 | ||||||
| chr1:44721513
|
T | TA | 8 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0069others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-2598dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44721513 | |||||
| chr1:44721513
|
TA | T | 9 | a0001c0001t0001g0052a0001c0001t0001g0098a0001c0001t0001g0161others(6): Show | 9 | HG00099.hp2 HG01192.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.725-2598delA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44721513 | |||||
| chr1:44721554
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.725-2568T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721554 | ||||||
| chr1:44721568
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-2554A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721568 | ||||||
| chr1:44721572
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.725-2550C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721572 | ||||||
| chr1:44721613
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.725-2509G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721613 | ||||||
| chr1:44721619
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.725-2503C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721619 | ||||||
| chr1:44721650
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0092 | 2 | NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.725-2472G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721650 | ||||||
| chr1:44721658
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(80): Show | 85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.725-2464G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721658 | ||||||
| chr1:44721665
|
G | A | 13 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.725-2457G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721665 | ||||||
| chr1:44721671
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-2451G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721671 | ||||||
| chr1:44721675
|
G | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(51): Show | 55 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.725-2447G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721675 | ||||||
| chr1:44721680
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.725-2442G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721680 | ||||||
| chr1:44721693
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.725-2429C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721693 | ||||||
| chr1:44721700
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.725-2422A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721700 | ||||||
| chr1:44721701
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0132a0001c0001t0001g0137others(3): Show | 6 | HG02015.hp1 HG02027.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-2421C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721701 | ||||||
| chr1:44721710
|
C | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-2412C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721710 | ||||||
| chr1:44721722
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.725-2400T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721722 | ||||||
| chr1:44721729
|
A | G | 1 | a0001c0001t0001g0008 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.725-2393A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721729 | ||||||
| chr1:44721730
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.725-2392C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721730 | ||||||
| chr1:44721735
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.725-2387C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721735 | ||||||
| chr1:44721741
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.725-2381A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721741 | ||||||
| chr1:44721743
|
G | T | 1 | a0001c0001t0001g0023 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.725-2379G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721743 | ||||||
| chr1:44721751
|
C | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-2371C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721751 | ||||||
| chr1:44721754
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.725-2368C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721754 | ||||||
| chr1:44721762
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.725-2360T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721762 | ||||||
| chr1:44721770
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.725-2352T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721770 | ||||||
| chr1:44721772
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0108others(3): Show | 6 | HG01167.hp1 HG01884.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-2350G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721772 | ||||||
| chr1:44721778
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0040others(4): Show | 7 | HG01099.hp1 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-2344G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721778 | ||||||
| chr1:44721783
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.725-2339T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721783 | ||||||
| chr1:44721787
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.725-2335G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721787 | ||||||
| chr1:44721789
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.725-2333C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721789 | ||||||
| chr1:44721794
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0077 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.725-2328C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721794 | ||||||
| chr1:44721795
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.725-2327T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721795 | ||||||
| chr1:44721797
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0199 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.725-2325G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721797 | ||||||
| chr1:44721798
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0216 | 2 | HG02965.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.725-2324G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721798 | ||||||
| chr1:44721802
|
G | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(12): Show | 17 | HG01123.hp1 HG01346.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.725-2320G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721802 | ||||||
| chr1:44721806
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0132a0001c0001t0001g0137others(4): Show | 7 | HG02015.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-2316T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721806 | ||||||
| chr1:44721807
|
C | CA | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-2309dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44721807 | |||||
| chr1:44721810
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.725-2312A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721810 | ||||||
| chr1:44721814
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0194 | 3 | HG01123.hp2 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.725-2308T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721814 | ||||||
| chr1:44721819
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.725-2303C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721819 | ||||||
| chr1:44721828
|
C | T | 1 | a0003c0002t0001g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.725-2294C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721828 | ||||||
| chr1:44721830
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.725-2292T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721830 | ||||||
| chr1:44721832
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(12): Show | 17 | HG01123.hp1 HG01346.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.725-2290G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721832 | ||||||
| chr1:44721839
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.725-2283T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721839 | ||||||
| chr1:44721840
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.725-2282T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721840 | ||||||
| chr1:44721841
|
C | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.725-2281C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721841 | ||||||
| chr1:44721844
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.725-2278C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721844 | ||||||
| chr1:44721844
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.725-2278C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721844 | ||||||
| chr1:44721849
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.725-2273A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721849 | ||||||
| chr1:44721859
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.725-2263T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721859 | ||||||
| chr1:44721867
|
G | A | 12 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(9): Show | 12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.725-2255G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721867 | ||||||
| chr1:44721877
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0083others(9): Show | 13 | HG01123.hp1 HG01346.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.725-2245T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721877 | ||||||
| chr1:44721879
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.725-2243C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721879 | ||||||
| chr1:44721880
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.725-2242G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721880 | ||||||
| chr1:44721881
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.725-2241T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721881 | ||||||
| chr1:44721885
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0241a0001c0001t0001g0275others(2): Show | 5 | HG01243.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-2237G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721885 | ||||||
| chr1:44721890
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.725-2232G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721890 | ||||||
| chr1:44721890
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.725-2232G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721890 | ||||||
| chr1:44721894
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.725-2228C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721894 | ||||||
| chr1:44721895
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.725-2227C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721895 | ||||||
| chr1:44721897
|
G | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(8): Show | 11 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.725-2225G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721897 | ||||||
| chr1:44721899
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0022others(17): Show | 22 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.725-2223G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721899 | ||||||
| chr1:44721900
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.725-2222A>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721900 | ||||||
| chr1:44721902
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.725-2220C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721902 | ||||||
| chr1:44721904
|
G | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0064a0001c0001t0001g0068others(12): Show | 15 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.725-2218G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721904 | ||||||
| chr1:44721905
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0227 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.725-2217C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721905 | ||||||
| chr1:44721906
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0071others(15): Show | 19 | HG01123.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.725-2216C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721906 | ||||||
| chr1:44721907
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.725-2215T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721907 | ||||||
| chr1:44721907
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.725-2215T>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721907 | ||||||
| chr1:44721912
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0018 | 3 | HG01261.hp2 HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.725-2210G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721912 | ||||||
| chr1:44721912
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.725-2210G>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721912 | ||||||
| chr1:44722037
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.725-2085C>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722037 | ||||||
| chr1:44722082
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-2040A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722082 | ||||||
| chr1:44722163
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.725-1959C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722163 | ||||||
| chr1:44722319
|
A | T | 1 | a0001c0001t0001g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.725-1803A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722319 | ||||||
| chr1:44722485
|
TCACTTTG others(4): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.725-1625_725-1615d others(13): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44722485 | |||||
| chr1:44722656
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-1466A>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722656 | ||||||
| chr1:44722903
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(112): Show | 118 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.725-1198dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44722903 | |||||
| chr1:44722903
|
C | CAA | 13 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0036others(10): Show | 13 | HG00735.hp2 HG01123.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.725-1199_725-1198d others(4): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44722903 | |||||
| chr1:44722903
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.725-1207_725-1198d others(12): Show |
ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44722903 | |||||
| chr1:44722946
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.725-1176C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44722946 | ||||||
| chr1:44723074
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.725-1034dupA | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 44723074 | |||||
| chr1:44723301
|
G | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.725-821G>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44723301 | ||||||
| chr1:44723316
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.725-806G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44723316 | ||||||
| chr1:44723401
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.725-721T>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44723401 | ||||||
| chr1:44723489
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.725-633C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44723489 | ||||||
| chr1:44724090
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.725-32G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44724090 | ||||||
| chr1:44724093
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.725-29C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44724093 | ||||||
| chr1:44724421
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+29G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 8/11 | chr1 | 44724421 | ||||||
| chr1:44724461
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.920+69C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 8/11 | chr1 | 44724461 | ||||||
| chr1:44725088
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1129-48C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 10/11 | chr1 | 44725088 | ||||||
| chr1:44725250
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0220 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1210+33C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 11/11 | chr1 | 44725250 | ||||||
| chr1:44725275
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1211-16C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 11/11 | chr1 | 44725275 |