Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MTSIK others(435): Show |
chr1 | 44669714 | 44730591 |
| a0002 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | MTSIK others(435): Show |
chr1 | 44669714 | 44730591 |
| a0003 | 0/0 | 440 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | MTSIK others(435): Show |
chr1 | 44669714 | 44730591 |
| a0004 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | MTSIK others(435): Show |
chr1 | 44669714 | 44730591 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1320 | 280 | 81 | 64 | 92 | 9 | 32 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
chr1 | 44669714 | 44730591 | ||
| a0001c0004 | 0/0 | 1320 | 2 | 0 | 1 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
chr1 | 44669714 | 44730591 | ||
| a0001c0006 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
chr1 | 44669714 | 44730591 | ||
| a0002c0002 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
chr1 | 44669714 | 44730591 | ||
| a0003c0003 | 0/0 | 1320 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
chr1 | 44669714 | 44730591 | ||
| a0004c0005 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | ATGAC others(1315): Show |
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 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0001c0001t0002 | 0/0 | 1693 | 4 | 3 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0001c0001t0003 | 0/0 | 1693 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0001c0004t0001 | 0/0 | 1693 | 2 | 0 | 1 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0001c0006t0001 | 0/0 | 1693 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0002c0002t0001 | 0/0 | 1693 | 2 | 0 | 2 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0003c0003t0001 | 0/0 | 1693 | 2 | 1 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| a0004c0005t0001 | 0/0 | 1693 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | GTAGG others(1688): Show |
chr1 | 44669714 | 44730591 |
| actghapid | grch38/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 | 1/0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| a0004c0005t0001g0169 | 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 | g0169 | 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 | g0259 | 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 | g0248 | 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 | g0250 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0257 | 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 | a0002 | 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 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0251 | 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 | a0003 | c0003 | t0001 | g0202 | AMR | PUR | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0176 | 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 | g0261 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | 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 | g0160 | 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 | g0161 | 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 | g0256 | AMR | CLM | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01516 | hp1 | a0001 | c0006 | t0001 | g0262 | EUR | IBS | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | 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 | g0255 | 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 | g0181 | 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 | g0178 | 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 | g0179 | 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 | g0167 | 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 | g0170 | 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 | g0258 | 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 | g0163 | SAS | PJL | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0263 | 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 | g0254 | 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 | g0173 | 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 | g0253 | 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 | g0252 | 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 | a0003 | 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 | g0180 | 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 | g0165 | 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 | g0171 | EAS | JPT | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0175 | 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 | g0174 | 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 | g0166 | 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 | g0164 | 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 | g0249 | 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 | g0177 | 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 | g0172 | 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 | a0001 | c0001 | t0001 | g0247 | REF | REF | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0159 | REF | REF | ARMH1_chr1_44669714_44730591 | ARMH1 | chr1 | 44669714 | 44730591 |
| view | 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 | a0002 | 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 | a0003 | 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 | a0003 | 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 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0184 others(87): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): 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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
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 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): 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 | a0001c0001t0001g0009 a0001c0001t0001g0183 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-23+1612G>A | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44676485 | |||||||
| chr1:44676537 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): 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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0017 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-23+4305T>C | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 1/11 | chr1 | 44679178 | |||||||
| chr1:44679184 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): 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 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | |||||||
| chr1:44680166 | A | AGTTT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0181 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0017 |
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 | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(92): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | 42 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0224 others(39): Show |
43 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(40): 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 | a0001c0001t0001g0250 | 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 | a0003c0003t0001g0274 | 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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0017 a0003c0003t0001g0274 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0265 a0002c0002t0001g0264 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
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 | a0001c0001t0001g0251 | 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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0181 a0004c0005t0001g0169 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | 43 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0183 others(40): Show |
44 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(41): 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | a0003c0003t0001g0274 | 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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | |||||||
| chr1:44689164 | G | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0014 a0001c0001t0002g0011 a0001c0001t0002g0222 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
134 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(131): 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
134 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.207-1221C>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 2/11 | chr1 | 44695881 | |||||||
| chr1:44695944 | CA | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
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 | a0003c0003t0001g0274 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | 30 | a0001c0001t0001g0066 a0001c0001t0001g0108 a0001c0001t0001g0162 others(27): Show |
30 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(27): 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0070 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | 28 | a0001c0001t0001g0066 a0001c0001t0001g0156 a0001c0001t0001g0162 others(25): Show |
28 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(25): 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 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0229 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0221 a0001c0001t0001g0229 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0229 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0042 others(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 | a0002c0002t0001g0136 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0259 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0002c0002t0001g0136 a0002c0002t0001g0264 |
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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0001g0212 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0229 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0229 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0217 |
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 | a0001c0001t0001g0221 a0001c0004t0001g0111 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0217 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0001g0217 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0104 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0071 others(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 | 3 | a0001c0001t0001g0050 a0001c0001t0001g0258 a0001c0006t0001g0262 |
3 | HG01516.hp1 HG02683.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.724+5368A>G | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44709541 | |||||||
| chr1:44709542 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | 7 | a0001c0001t0001g0050 a0001c0001t0001g0097 a0001c0001t0001g0139 others(4): Show |
7 | HG01516.hp1 HG02683.hp2 HG03492.hp2 others(4): 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 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0240 |
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 | 4 | a0001c0001t0001g0050 a0001c0001t0001g0255 a0001c0001t0001g0258 others(1): Show |
4 | HG01516.hp1 HG01993.hp1 HG02683.hp2 others(1): 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 | a0001c0001t0001g0009 a0001c0001t0001g0183 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0193 |
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 | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): 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 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0168 | 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): 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 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): 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 | a0001c0001t0001g0006 a0001c0001t0001g0094 |
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 | 4 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01256.hp2 others(1): 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 | a0001c0001t0001g0071 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0041 others(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 | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
98 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(95): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0229 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0025 others(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 | 10 | a0001c0001t0001g0096 a0001c0001t0001g0125 a0001c0001t0001g0144 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(7): 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 | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): 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 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0220 a0001c0001t0001g0221 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0175 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0165 | 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 | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(78): Show |
83 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(80): 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 | a0001c0001t0001g0023 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0058 others(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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(86): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): 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 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): 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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(106): 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 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0240 |
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 | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(79): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): 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 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0001g0118 others(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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): 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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.725-2550C>T | ARMH1 | ENSG00000198520.12 | transcript | ENST00000535358.6 | protein_coding | 6/11 | chr1 | 44721572 | |||||||
| chr1:44721613 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0092 |
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 | 82 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0077 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0216 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0194 |
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 | a0002c0002t0001g0264 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0035 others(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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): 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 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0241 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(111): Show |
117 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(114): 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 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(80): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0220 |
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 |