Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 150280 |
|---|---|
| ensemblid | ENSG00000176635.18 |
| hgncid | 28383 |
| symbol | HORMAD2 |
| name | HORMA domain containing 2 |
| refseq_nuc | NM_152510.4 |
| refseq_prot | NP_689723.1 |
| ensembl_nuc | ENST00000336726.11 |
| ensembl_prot | ENSP00000336984.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 30080464 |
| end | 30177075 |
| strand | + |
| ver | v1.2 |
| region | chr22:30080464-30177075 |
| region5000 | chr22:30075464-30182075 |
| regionname0 | HORMAD2_chr22_30080464_30177075 |
| regionname5000 | HORMAD2_chr22_30075464_30182075 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 307 | 343 | 89 | 70 | 140 | 12 | 30 | 102 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0002 | 0/0 | 307 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0003 | 0/0 | 307 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0004 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 924 | 343 | 89 | 70 | 140 | 12 | 30 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| c0002 | 0/0 | 924 | 5 | 4 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| c0003 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| c0004 | 0/0 | 924 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 974 | 299 | 81 | 62 | 120 | 11 | 23 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| t0002 | 0/0 | 974 | 46 | 8 | 10 | 20 | 1 | 7 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| t0003 | 0/0 | 974 | 3 | 3 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| t0004 | 0/0 | 974 | 2 | 2 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 924 | 343 | 89 | 70 | 140 | 12 | 30 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0002c0002 | 0/0 | 924 | 5 | 4 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0003c0004 | 0/0 | 924 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0004c0003 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1897 | 292 | 76 | 60 | 120 | 11 | 23 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0001c0001t0002 | 0/0 | 1897 | 46 | 8 | 10 | 20 | 1 | 7 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0001c0001t0003 | 0/0 | 1897 | 3 | 3 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0001c0001t0004 | 0/0 | 1897 | 2 | 2 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0002c0002t0001 | 0/0 | 1897 | 5 | 4 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0003c0004t0001 | 0/0 | 1897 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| a0004c0003t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | copy fasta | chr22 | 30075464 | 30182075 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0003c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| a0004c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | FIN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | FIN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0272 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CDX | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03130 | hp1 | a0004 | c0003 | t0001 | g0008 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ASW | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | TSI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | USA | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | USA | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | USA | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0298 | REF | REF | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0246 | REF | REF | HORMAD2_chr22_30075464_30182075 | HORMAD2 | chr22 | 30075464 | 30182075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30098858
|
G | C | 1 | a0002 | 5 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.58G>C | p.Val20Leu | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/11 | 123/1897 | 58/924 | 20/307 | chr22 | 30098858 | ||
| chr22:30121718
|
T | C | 1 | a0004 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.497T>C | p.Ile166Thr | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 9/11 | 562/1897 | 497/924 | 166/307 | chr22 | 30121718 | ||
| chr22:30122177
|
G | A | 1 | a0003 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.782G>A | p.Gly261Asp | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/11 | 847/1897 | 782/924 | 261/307 | chr22 | 30122177 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30176203
|
A | C | 1 | a0001c0001t0003 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*36A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 11/11 | 36 | chr22 | 30176203 | |||||
| chr22:30176350
|
C | T | 1 | a0001c0001t0003 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 11/11 | 183 | chr22 | 30176350 | |||||
| chr22:30176747
|
G | A | 1 | a0001c0001t0002 | 46 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*580G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 11/11 | 580 | chr22 | 30176747 | |||||
| chr22:30177002
|
A | G | 2 | a0001c0001t0003a0001c0001t0004 | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*835A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 11/11 | 835 | chr22 | 30177002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30080572
|
A | T | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38+81A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30080572 | ||||||
| chr22:30080803
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-38+312C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30080803 | ||||||
| chr22:30081253
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-38+762G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081253 | ||||||
| chr22:30081583
|
C | CT | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0265others(56): Show | 60 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-38+1102dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30081583 | |||||
| chr22:30081600
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 242 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.-38+1109T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081600 | ||||||
| chr22:30081685
|
C | G | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+1194C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081685 | ||||||
| chr22:30081689
|
C | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-38+1198C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081689 | ||||||
| chr22:30081837
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+1346G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081837 | ||||||
| chr22:30081982
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38+1491T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30081982 | ||||||
| chr22:30082126
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+1635A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082126 | ||||||
| chr22:30082189
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38+1698T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082189 | ||||||
| chr22:30082267
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-38+1776T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082267 | ||||||
| chr22:30082450
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+1959C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082450 | ||||||
| chr22:30082473
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38+1982A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082473 | ||||||
| chr22:30082547
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+2056T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082547 | ||||||
| chr22:30082606
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+2115C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082606 | ||||||
| chr22:30082616
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38+2125A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082616 | ||||||
| chr22:30082671
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-38+2180A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082671 | ||||||
| chr22:30082742
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+2251T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082742 | ||||||
| chr22:30082778
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+2287C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082778 | ||||||
| chr22:30082795
|
C | CA | 59 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(56): Show | 59 | HG00280.hp1 HG00597.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-38+2318dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30082795 | |||||
| chr22:30082795
|
CA | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0153a0001c0001t0001g0154others(11): Show | 14 | HG00639.hp1 HG01256.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+2318delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30082795 | |||||
| chr22:30082961
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+2470G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30082961 | ||||||
| chr22:30083282
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-38+2791G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30083282 | ||||||
| chr22:30083594
|
A | AGAATAAT others(8): Show |
1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+3107_-38+3121d others(17): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30083594 | |||||
| chr22:30083628
|
T | A | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-38+3137T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30083628 | ||||||
| chr22:30083680
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-38+3189A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30083680 | ||||||
| chr22:30083685
|
G | A | 7 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+3194G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30083685 | ||||||
| chr22:30084641
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-38+4150T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30084641 | ||||||
| chr22:30084953
|
C | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-38+4462C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30084953 | ||||||
| chr22:30085128
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+4637A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085128 | ||||||
| chr22:30085145
|
C | CA | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-38+4668dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30085145 | |||||
| chr22:30085430
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+4939T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085430 | ||||||
| chr22:30085440
|
C | T | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-38+4949C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085440 | ||||||
| chr22:30085442
|
C | T | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG01943.hp1 HG01981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-38+4951C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085442 | ||||||
| chr22:30085652
|
G | A | 38 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(35): Show | 38 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.-38+5161G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085652 | ||||||
| chr22:30085869
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(43): Show | 47 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.-38+5378C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30085869 | ||||||
| chr22:30086172
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-38+5681G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086172 | ||||||
| chr22:30086272
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-38+5781A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086272 | ||||||
| chr22:30086329
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18969.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.-38+5838A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086329 | ||||||
| chr22:30086784
|
G | GAT | 4 | a0001c0001t0001g0121a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 4 | HG01934.hp1 HG01993.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+6308_-38+6309d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30086784 | |||||
| chr22:30086837
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-38+6346C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086837 | ||||||
| chr22:30086848
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-38+6357G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086848 | ||||||
| chr22:30086951
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.-38+6460C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30086951 | ||||||
| chr22:30087394
|
G | C | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-37-6522G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087394 | ||||||
| chr22:30087401
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-6515G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087401 | ||||||
| chr22:30087706
|
GGAGA | G | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG00423.hp1 HG01934.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37-6198_-37-6195d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30087706 | |||||
| chr22:30087722
|
GA | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-6183delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30087722 | |||||
| chr22:30087745
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-6171C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087745 | ||||||
| chr22:30087775
|
A | C | 1 | a0001c0001t0001g0300 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-37-6141A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087775 | ||||||
| chr22:30087776
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-37-6140C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087776 | ||||||
| chr22:30087962
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-37-5954T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087962 | ||||||
| chr22:30087973
|
C | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-5943C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087973 | ||||||
| chr22:30087975
|
C | A | 80 | a0001c0001t0001g0007a0001c0001t0001g0085a0001c0001t0001g0086others(77): Show | 80 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-37-5941C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087975 | ||||||
| chr22:30087977
|
A | C | 99 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(96): Show | 99 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-37-5939A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087977 | ||||||
| chr22:30087979
|
A | C | 4 | a0001c0001t0002g0015a0001c0001t0002g0019a0001c0001t0002g0020others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5937A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30087979 | ||||||
| chr22:30088005
|
A | G | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-5911A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088005 | ||||||
| chr22:30088037
|
G | GTATACAT others(17): Show |
125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(122): Show | 125 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.-37-5873_-37-5872i others(26): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088037 | |||||
| chr22:30088044
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-5872C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088044 | ||||||
| chr22:30088046
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-5870C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088046 | ||||||
| chr22:30088057
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37-5859A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088057 | ||||||
| chr22:30088057
|
ATACATAT others(19): Show |
A | 2 | a0001c0001t0001g0261a0001c0001t0001g0263 | 2 | HG02027.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-37-5810_-37-5785d others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088057 | |||||
| chr22:30088098
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-5818C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088098 | ||||||
| chr22:30088106
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-37-5810C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088106 | ||||||
| chr22:30088106
|
CGTGTACA others(19): Show |
C | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-37-5794_-37-5769d others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088106 | |||||
| chr22:30088114
|
T | TACACACA others(15): Show |
4 | a0002c0002t0001g0054a0002c0002t0001g0070a0002c0002t0001g0071others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5801_-37-5800i others(24): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088114 | |||||
| chr22:30088118
|
C | CACACACA others(17): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01069.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-37-5792_-37-5791i others(26): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088118 | |||||
| chr22:30088118
|
C | CACACACA others(15): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG01167.hp1 HG01169.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-37-5792_-37-5791i others(24): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088118 | |||||
| chr22:30088118
|
C | CACACACA others(17): Show |
1 | a0002c0002t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-37-5792_-37-5791i others(26): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088118 | |||||
| chr22:30088118
|
C | T | 4 | a0002c0002t0001g0054a0002c0002t0001g0070a0002c0002t0001g0071others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5798C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088118 | ||||||
| chr22:30088125
|
G | A | 11 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(8): Show | 11 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-5791G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088125 | ||||||
| chr22:30088159
|
G | GTATACCT others(19): Show |
1 | a0001c0001t0001g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-5725_-37-5700d others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088159 | |||||
| chr22:30088162
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-37-5754T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088162 | ||||||
| chr22:30088166
|
T | TATGTATA others(19): Show |
4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-5725_-37-5724i others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088166 | |||||
| chr22:30088184
|
T | C | 30 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0187others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-37-5732T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088184 | ||||||
| chr22:30088203
|
A | G | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-5713A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088203 | ||||||
| chr22:30088616
|
TTAAG | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-5294_-37-5291d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30088616 | |||||
| chr22:30088978
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-37-4938G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30088978 | ||||||
| chr22:30089093
|
A | G | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.-37-4823A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089093 | ||||||
| chr22:30089351
|
G | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0074others(41): Show | 44 | HG00423.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-37-4565G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089351 | ||||||
| chr22:30089354
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-37-4562T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089354 | ||||||
| chr22:30089355
|
C | CT | 49 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0074others(46): Show | 49 | HG01069.hp1 HG01099.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-37-4546dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30089355 | |||||
| chr22:30089357
|
T | TC | 26 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(23): Show | 26 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-37-4559_-37-4558i others(3): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089357 | ||||||
| chr22:30089412
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0318 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-37-4504G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089412 | ||||||
| chr22:30089508
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-37-4408A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089508 | ||||||
| chr22:30089540
|
A | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG00558.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-37-4376A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089540 | ||||||
| chr22:30089548
|
T | G | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-4368T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089548 | ||||||
| chr22:30089598
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-37-4318G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089598 | ||||||
| chr22:30089651
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-37-4265G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089651 | ||||||
| chr22:30089845
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-37-4071C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089845 | ||||||
| chr22:30089864
|
C | T | 31 | a0001c0001t0001g0066a0001c0001t0001g0122a0001c0001t0001g0123others(28): Show | 31 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-37-4052C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30089864 | ||||||
| chr22:30090064
|
T | G | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-3852T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090064 | ||||||
| chr22:30090117
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-37-3799C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090117 | ||||||
| chr22:30090118
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-37-3798A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090118 | ||||||
| chr22:30090223
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-3693T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090223 | ||||||
| chr22:30090497
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-37-3419A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090497 | ||||||
| chr22:30090534
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-37-3382G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090534 | ||||||
| chr22:30090593
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-37-3323G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090593 | ||||||
| chr22:30090837
|
A | G | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.-37-3079A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090837 | ||||||
| chr22:30090866
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-37-3050A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30090866 | ||||||
| chr22:30091021
|
A | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-2895A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091021 | ||||||
| chr22:30091076
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-2840G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091076 | ||||||
| chr22:30091078
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37-2838A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091078 | ||||||
| chr22:30091254
|
CTCTCTTT others(6): Show |
C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-37-2660_-37-2648d others(15): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091254 | |||||
| chr22:30091254
|
CTCTCTTT others(8): Show |
C | 24 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0325others(21): Show | 24 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-37-2660_-37-2646d others(17): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091254 | |||||
| chr22:30091254
|
CTCTCTTT others(9): Show |
C | 1 | a0001c0001t0001g0324 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-37-2660_-37-2645d others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091254 | |||||
| chr22:30091262
|
CTTTCTT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2650_-37-2645d others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091262 | |||||
| chr22:30091266
|
CT | C | 82 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0073others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-37-2632delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091266 | |||||
| chr22:30091266
|
CTT | C | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG01934.hp2 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-2633_-37-2632d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091266 | |||||
| chr22:30091266
|
CTTT | C | 55 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.-37-2634_-37-2632d others(5): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30091266 | |||||
| chr22:30091270
|
T | C | 21 | a0001c0001t0001g0089a0001c0001t0001g0163a0001c0001t0001g0165others(18): Show | 21 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37-2646T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091270 | ||||||
| chr22:30091271
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-37-2645T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091271 | ||||||
| chr22:30091273
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.-37-2643T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091273 | ||||||
| chr22:30091437
|
C | T | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-37-2479C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091437 | ||||||
| chr22:30091630
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-2286G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091630 | ||||||
| chr22:30091911
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-2005C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30091911 | ||||||
| chr22:30092043
|
A | AT | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0117others(39): Show | 43 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-37-1855dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30092043 | |||||
| chr22:30092043
|
A | ATT | 23 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(20): Show | 23 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37-1856_-37-1855d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30092043 | |||||
| chr22:30092043
|
AT | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-37-1855delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30092043 | |||||
| chr22:30092147
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(39): Show | 43 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.-37-1769C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092147 | ||||||
| chr22:30092173
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-37-1743G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092173 | ||||||
| chr22:30092218
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0266others(45): Show | 48 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-37-1698G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092218 | ||||||
| chr22:30092297
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-37-1619T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092297 | ||||||
| chr22:30092308
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-37-1608A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092308 | ||||||
| chr22:30092345
|
C | CT | 133 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0062others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.-37-1554dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30092345 | |||||
| chr22:30092345
|
C | CTT | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0075others(8): Show | 12 | HG00639.hp1 HG01993.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.-37-1555_-37-1554d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 30092345 | |||||
| chr22:30092493
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-37-1423G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092493 | ||||||
| chr22:30092638
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.-37-1278G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092638 | ||||||
| chr22:30092685
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-1231G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092685 | ||||||
| chr22:30092737
|
A | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37-1179A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092737 | ||||||
| chr22:30092854
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00621.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-37-1062T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092854 | ||||||
| chr22:30092915
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-1001G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30092915 | ||||||
| chr22:30093302
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-37-614T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093302 | ||||||
| chr22:30093332
|
T | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-584T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093332 | ||||||
| chr22:30093464
|
A | G | 4 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 4 | HG01943.hp1 HG01981.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-452A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093464 | ||||||
| chr22:30093827
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-89T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093827 | ||||||
| chr22:30093844
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-37-72A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093844 | ||||||
| chr22:30093904
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-37-12A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 1/10 | chr22 | 30093904 | ||||||
| chr22:30094302
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.51+299T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094302 | ||||||
| chr22:30094311
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.51+308C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094311 | ||||||
| chr22:30094379
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+376C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094379 | ||||||
| chr22:30094432
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+429C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094432 | ||||||
| chr22:30094509
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51+506A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094509 | ||||||
| chr22:30094522
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.51+519C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094522 | ||||||
| chr22:30094593
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.51+590T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094593 | ||||||
| chr22:30094744
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.51+741T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094744 | ||||||
| chr22:30094765
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+762G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094765 | ||||||
| chr22:30094795
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+792C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094795 | ||||||
| chr22:30094913
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.51+910A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094913 | ||||||
| chr22:30094968
|
T | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0088others(4): Show | 7 | NA18945.hp1 NA18968.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+965T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30094968 | ||||||
| chr22:30095011
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG00733.hp2 HG00738.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.51+1008T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095011 | ||||||
| chr22:30095162
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.51+1159A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095162 | ||||||
| chr22:30095256
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.51+1253G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095256 | ||||||
| chr22:30095523
|
G | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.51+1520G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095523 | ||||||
| chr22:30095802
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.51+1799T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095802 | ||||||
| chr22:30095863
|
A | C | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+1860A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095863 | ||||||
| chr22:30095977
|
G | A | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.51+1974G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30095977 | ||||||
| chr22:30096054
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+2051A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096054 | ||||||
| chr22:30096250
|
T | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.51+2247T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096250 | ||||||
| chr22:30096311
|
A | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 92 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.51+2308A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096311 | ||||||
| chr22:30096366
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.51+2363A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096366 | ||||||
| chr22:30096481
|
A | AT | 52 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(49): Show | 53 | HG00558.hp1 HG01168.hp1 HG01169.hp1 others(50): Show |
intron_variant | MODIFIER | c.52-2358dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr22 | 30096481 | |||||
| chr22:30096550
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.52-2302C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096550 | ||||||
| chr22:30096633
|
A | G | 1 | a0001c0001t0001g0004 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.52-2219A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096633 | ||||||
| chr22:30096758
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-2094C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096758 | ||||||
| chr22:30096789
|
A | T | 25 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(22): Show | 25 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.52-2063A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096789 | ||||||
| chr22:30096857
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01081.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.52-1995C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30096857 | ||||||
| chr22:30097102
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52-1750A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097102 | ||||||
| chr22:30097130
|
A | G | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52-1722A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097130 | ||||||
| chr22:30097134
|
T | G | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.52-1718T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097134 | ||||||
| chr22:30097332
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-1520C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097332 | ||||||
| chr22:30097571
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-1281A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097571 | ||||||
| chr22:30097725
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG00642.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.52-1127A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097725 | ||||||
| chr22:30097763
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.52-1089A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097763 | ||||||
| chr22:30097891
|
T | G | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52-961T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097891 | ||||||
| chr22:30097893
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.52-959G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097893 | ||||||
| chr22:30097929
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 45 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.52-923A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097929 | ||||||
| chr22:30097930
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.52-922T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30097930 | ||||||
| chr22:30098114
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.52-738T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098114 | ||||||
| chr22:30098330
|
A | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-522A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098330 | ||||||
| chr22:30098382
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.52-470G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098382 | ||||||
| chr22:30098506
|
T | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.52-346T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098506 | ||||||
| chr22:30098544
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG01069.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.52-308G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098544 | ||||||
| chr22:30098653
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.52-199T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098653 | ||||||
| chr22:30098667
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52-185T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098667 | ||||||
| chr22:30098800
|
A | C | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.52-52A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 2/10 | chr22 | 30098800 | ||||||
| chr22:30099091
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193+98C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099091 | ||||||
| chr22:30099195
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.193+202G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099195 | ||||||
| chr22:30099261
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193+268C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099261 | ||||||
| chr22:30099342
|
G | A | 1 | a0003c0004t0001g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.193+349G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099342 | ||||||
| chr22:30099386
|
G | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.193+393G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099386 | ||||||
| chr22:30099756
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.193+763G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30099756 | ||||||
| chr22:30100109
|
AG | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 59 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.193+1118delG | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr22 | 30100109 | |||||
| chr22:30100263
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+1270G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30100263 | ||||||
| chr22:30100700
|
A | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG00597.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.193+1707A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30100700 | ||||||
| chr22:30100853
|
TAGAG | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193+1864_193+1867d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr22 | 30100853 | |||||
| chr22:30100921
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.193+1928A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30100921 | ||||||
| chr22:30101097
|
T | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(340): Show | 347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.193+2104T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30101097 | ||||||
| chr22:30101500
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.194-1937T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30101500 | ||||||
| chr22:30101724
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.194-1713A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30101724 | ||||||
| chr22:30101739
|
G | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-1698G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30101739 | ||||||
| chr22:30102195
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.194-1242T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102195 | ||||||
| chr22:30102551
|
A | C | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.194-886A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102551 | ||||||
| chr22:30102561
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-876G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102561 | ||||||
| chr22:30102630
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.194-807A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102630 | ||||||
| chr22:30102668
|
G | A | 4 | a0001c0001t0001g0190a0001c0001t0003g0160a0001c0001t0003g0161others(1): Show | 4 | HG03098.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-769G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102668 | ||||||
| chr22:30102711
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0154 | 4 | HG01256.hp2 HG01258.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-726G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102711 | ||||||
| chr22:30102907
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-530G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102907 | ||||||
| chr22:30102908
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00423.hp1 HG01981.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.194-529G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102908 | ||||||
| chr22:30102989
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-448G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30102989 | ||||||
| chr22:30103104
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-333G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103104 | ||||||
| chr22:30103152
|
C | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.194-285C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103152 | ||||||
| chr22:30103152
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194-285C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103152 | ||||||
| chr22:30103237
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.194-200G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103237 | ||||||
| chr22:30103334
|
T | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.194-103T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103334 | ||||||
| chr22:30103409
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.194-28A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 3/10 | chr22 | 30103409 | ||||||
| chr22:30103649
|
A | AT | 45 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(42): Show | 46 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.257+180dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATT | 18 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.257+179_257+180dup others(2): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTT | 10 | a0001c0001t0001g0066a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG01099.hp1 HG01981.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+178_257+180dup others(3): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTT | 13 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0122others(10): Show | 13 | HG00423.hp1 HG01192.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.257+177_257+180dup others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTT | 27 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0145others(24): Show | 27 | HG00280.hp1 HG01934.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.257+176_257+180dup others(5): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTTT | 15 | a0001c0001t0001g0148a0001c0001t0001g0325a0001c0001t0001g0345others(12): Show | 15 | HG01358.hp2 HG01943.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+175_257+180dup others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTTTT | 16 | a0001c0001t0001g0083a0001c0001t0001g0322a0001c0001t0001g0324others(13): Show | 16 | HG00597.hp2 HG01123.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+174_257+180dup others(7): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTTTT others(1): Show |
15 | a0001c0001t0001g0323a0001c0001t0001g0331a0001c0001t0001g0332others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+173_257+180dup others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0080 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.257+170_257+180dup others(11): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.257+167_257+180dup others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
AT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0056others(33): Show | 37 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.257+180delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
ATT | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0064others(46): Show | 49 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.257+179_257+180del others(2): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
ATTT | A | 14 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.257+178_257+180del others(3): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0261 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.257+171_257+180del others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103649
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.257+168_257+180del others(13): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 30103649 | |||||
| chr22:30103723
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.257+223C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30103723 | ||||||
| chr22:30103724
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.257+224G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30103724 | ||||||
| chr22:30103804
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.257+304G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30103804 | ||||||
| chr22:30103953
|
C | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-448C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30103953 | ||||||
| chr22:30104099
|
T | C | 9 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(6): Show | 9 | HG00639.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-302T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30104099 | ||||||
| chr22:30104245
|
A | G | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG00733.hp2 HG00738.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.258-156A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30104245 | ||||||
| chr22:30104300
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.258-101T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 4/10 | chr22 | 30104300 | ||||||
| chr22:30104446
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+9G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30104446 | ||||||
| chr22:30104664
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.294+227C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30104664 | ||||||
| chr22:30104717
|
G | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+280G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30104717 | ||||||
| chr22:30104905
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.294+468A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30104905 | ||||||
| chr22:30104969
|
G | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 59 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.294+532G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30104969 | ||||||
| chr22:30105116
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+679C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30105116 | ||||||
| chr22:30105497
|
T | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(49): Show | 53 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.294+1060T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30105497 | ||||||
| chr22:30105642
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.294+1205T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30105642 | ||||||
| chr22:30105915
|
G | A | 6 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+1478G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30105915 | ||||||
| chr22:30106773
|
A | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+2336A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30106773 | ||||||
| chr22:30107018
|
G | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 248 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.294+2581G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107018 | ||||||
| chr22:30107038
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG01884.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.294+2601A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107038 | ||||||
| chr22:30107182
|
G | A | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 195 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.294+2745G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107182 | ||||||
| chr22:30107223
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(49): Show | 53 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.294+2786A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107223 | ||||||
| chr22:30107264
|
A | T | 46 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(43): Show | 46 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.294+2827A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107264 | ||||||
| chr22:30107316
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.294+2879C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107316 | ||||||
| chr22:30107700
|
A | G | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+3263A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107700 | ||||||
| chr22:30107729
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0046 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.294+3292G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107729 | ||||||
| chr22:30107838
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0235 | 3 | HG01106.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.294+3401A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107838 | ||||||
| chr22:30107872
|
A | AT | 52 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(49): Show | 52 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.294+3449dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30107872 | |||||
| chr22:30107872
|
AT | A | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 41 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.294+3449delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30107872 | |||||
| chr22:30107891
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+3454C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107891 | ||||||
| chr22:30107892
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+3455G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30107892 | ||||||
| chr22:30108001
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.294+3564T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30108001 | ||||||
| chr22:30108122
|
C | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00280.hp1 HG00597.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.295-3674C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30108122 | ||||||
| chr22:30108218
|
A | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 60 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.295-3578A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30108218 | ||||||
| chr22:30108663
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.295-3133A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30108663 | ||||||
| chr22:30108866
|
T | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-2930T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30108866 | ||||||
| chr22:30108913
|
GCTCT | G | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.295-2878_295-2875d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30108913 | |||||
| chr22:30109013
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-2783C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109013 | ||||||
| chr22:30109129
|
AT | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-2665delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30109129 | |||||
| chr22:30109157
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.295-2639T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109157 | ||||||
| chr22:30109179
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.295-2617T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109179 | ||||||
| chr22:30109269
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0088others(2): Show | 5 | NA18968.hp2 NA18999.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-2527C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109269 | ||||||
| chr22:30109443
|
A | G | 2 | a0001c0001t0002g0019a0001c0001t0002g0021 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.295-2353A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109443 | ||||||
| chr22:30109657
|
A | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-2139A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109657 | ||||||
| chr22:30109763
|
T | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-2033T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30109763 | ||||||
| chr22:30110155
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-1641T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110155 | ||||||
| chr22:30110351
|
C | G | 2 | a0001c0001t0001g0009a0004c0003t0001g0008 | 2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.295-1445C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110351 | ||||||
| chr22:30110383
|
CT | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.295-1393delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30110383 | |||||
| chr22:30110383
|
CTT | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0129others(7): Show | 10 | HG01070.hp1 HG01943.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-1394_295-1393d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30110383 | |||||
| chr22:30110789
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.295-1007T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110789 | ||||||
| chr22:30110804
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.295-992A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110804 | ||||||
| chr22:30110804
|
A | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.295-992A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110804 | ||||||
| chr22:30110882
|
G | A | 1 | a0001c0001t0001g0004 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.295-914G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110882 | ||||||
| chr22:30110939
|
C | T | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0243others(3): Show | 6 | NA18968.hp1 NA18977.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-857C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30110939 | ||||||
| chr22:30111015
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.295-781G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111015 | ||||||
| chr22:30111030
|
C | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-766C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111030 | ||||||
| chr22:30111152
|
C | CA | 88 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0121others(85): Show | 88 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.295-627dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 30111152 | |||||
| chr22:30111342
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-454C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111342 | ||||||
| chr22:30111343
|
G | A | 2 | a0002c0002t0001g0070a0002c0002t0001g0071 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.295-453G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111343 | ||||||
| chr22:30111346
|
C | T | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-450C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111346 | ||||||
| chr22:30111369
|
G | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 250 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.295-427G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111369 | ||||||
| chr22:30111530
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA19084.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.295-266C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 5/10 | chr22 | 30111530 | ||||||
| chr22:30111845
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.315+29C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30111845 | ||||||
| chr22:30111950
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315+134T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30111950 | ||||||
| chr22:30112001
|
T | C | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.315+185T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112001 | ||||||
| chr22:30112256
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-240A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112256 | ||||||
| chr22:30112257
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.316-239T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112257 | ||||||
| chr22:30112286
|
C | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(160): Show | 164 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.316-210C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112286 | ||||||
| chr22:30112348
|
A | G | 1 | a0004c0003t0001g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.316-148A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112348 | ||||||
| chr22:30112418
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.316-78C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 6/10 | chr22 | 30112418 | ||||||
| chr22:30112594
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.342+72G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30112594 | ||||||
| chr22:30112794
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.342+272A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30112794 | ||||||
| chr22:30113050
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.342+528C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113050 | ||||||
| chr22:30113410
|
T | C | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.342+888T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113410 | ||||||
| chr22:30113487
|
C | T | 23 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 23 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.342+965C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113487 | ||||||
| chr22:30113508
|
GATTACTG others(9): Show |
G | 1 | a0001c0001t0001g0182 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.342+988_342+1003de others(17): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 30113508 | |||||
| chr22:30113510
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.342+988T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113510 | ||||||
| chr22:30113558
|
A | C | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0319 | 3 | HG02976.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.342+1036A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113558 | ||||||
| chr22:30113702
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.342+1180T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113702 | ||||||
| chr22:30113853
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.342+1331C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113853 | ||||||
| chr22:30113863
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.342+1341C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113863 | ||||||
| chr22:30113873
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.342+1351A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30113873 | ||||||
| chr22:30114076
|
T | C | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+1554T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114076 | ||||||
| chr22:30114257
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.342+1735T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114257 | ||||||
| chr22:30114260
|
A | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 92 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.342+1738A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114260 | ||||||
| chr22:30114432
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.342+1910A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114432 | ||||||
| chr22:30114671
|
A | T | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.342+2149A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114671 | ||||||
| chr22:30114707
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.342+2185A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114707 | ||||||
| chr22:30114724
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.342+2202T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30114724 | ||||||
| chr22:30115003
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.342+2481C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30115003 | ||||||
| chr22:30115192
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.342+2670T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30115192 | ||||||
| chr22:30115317
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.342+2795G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30115317 | ||||||
| chr22:30115750
|
G | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.342+3228G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30115750 | ||||||
| chr22:30116089
|
A | ATAT | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-2881_343-2879d others(5): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 30116089 | |||||
| chr22:30116139
|
G | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0219a0001c0001t0001g0265others(46): Show | 49 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.343-2841G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116139 | ||||||
| chr22:30116210
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.343-2770G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116210 | ||||||
| chr22:30116257
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.343-2723A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116257 | ||||||
| chr22:30116269
|
G | A | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 195 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.343-2711G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116269 | ||||||
| chr22:30116425
|
C | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 60 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.343-2555C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116425 | ||||||
| chr22:30116459
|
C | T | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.343-2521C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116459 | ||||||
| chr22:30116489
|
G | A | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 195 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.343-2491G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116489 | ||||||
| chr22:30116751
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.343-2229A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116751 | ||||||
| chr22:30116801
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.343-2179T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116801 | ||||||
| chr22:30116929
|
G | A | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.343-2051G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116929 | ||||||
| chr22:30116936
|
C | CT | 26 | a0001c0001t0001g0083a0001c0001t0001g0322a0001c0001t0001g0323others(23): Show | 26 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-2043dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 30116936 | |||||
| chr22:30116976
|
G | C | 1 | a0001c0001t0001g0304 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.343-2004G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30116976 | ||||||
| chr22:30117129
|
A | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-1851A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30117129 | ||||||
| chr22:30117454
|
GTTATT | G | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.343-1519_343-1515d others(7): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 30117454 | |||||
| chr22:30117575
|
C | G | 23 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 23 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.343-1405C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30117575 | ||||||
| chr22:30117634
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.343-1346G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30117634 | ||||||
| chr22:30118000
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0210 | 2 | NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.343-980A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118000 | ||||||
| chr22:30118177
|
C | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00558.hp1 NA18962.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-803C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118177 | ||||||
| chr22:30118310
|
C | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0013a0004c0003t0001g0008 | 3 | HG02622.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.343-670C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118310 | ||||||
| chr22:30118350
|
C | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025 | 3 | HG01934.hp1 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.343-630C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118350 | ||||||
| chr22:30118356
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0210 | 2 | NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.343-624T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118356 | ||||||
| chr22:30118491
|
G | A | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.343-489G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118491 | ||||||
| chr22:30118564
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-416T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118564 | ||||||
| chr22:30118600
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.343-380G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118600 | ||||||
| chr22:30118704
|
T | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-276T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 7/10 | chr22 | 30118704 | ||||||
| chr22:30119060
|
T | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.410+13T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119060 | ||||||
| chr22:30119064
|
T | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+17T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119064 | ||||||
| chr22:30119118
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.410+71G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119118 | ||||||
| chr22:30119386
|
G | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.410+339G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119386 | ||||||
| chr22:30119711
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+664G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119711 | ||||||
| chr22:30119781
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.410+734A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119781 | ||||||
| chr22:30119993
|
A | G | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG00423.hp2 NA18942.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+946A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30119993 | ||||||
| chr22:30120151
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.410+1104T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120151 | ||||||
| chr22:30120480
|
C | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG00642.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.411-1152C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120480 | ||||||
| chr22:30120544
|
A | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-1088A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120544 | ||||||
| chr22:30120636
|
TA | T | 46 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(43): Show | 46 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.411-994delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 30120636 | |||||
| chr22:30120897
|
TGGGCAAT others(6): Show |
T | 1 | a0001c0001t0001g0182 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.411-734_411-722del others(13): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120897 | ||||||
| chr22:30120938
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.411-694G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120938 | ||||||
| chr22:30120942
|
T | G | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.411-690T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120942 | ||||||
| chr22:30120958
|
TAC | T | 45 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 45 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.411-669_411-668del others(2): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 30120958 | |||||
| chr22:30120998
|
A | C | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-634A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30120998 | ||||||
| chr22:30121105
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.411-527C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30121105 | ||||||
| chr22:30121336
|
G | A | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.411-296G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30121336 | ||||||
| chr22:30121341
|
G | A | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.411-291G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 8/10 | chr22 | 30121341 | ||||||
| chr22:30121864
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.568+75G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 9/10 | chr22 | 30121864 | ||||||
| chr22:30121960
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | splice_region_variant&intron_variant | LOW | c.569-4G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 9/10 | chr22 | 30121960 | ||||||
| chr22:30122244
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+30G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122244 | ||||||
| chr22:30122318
|
C | T | 3 | a0001c0001t0002g0028a0001c0001t0002g0039a0001c0001t0002g0040 | 3 | NA18949.hp2 NA18959.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.819+104C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122318 | ||||||
| chr22:30122513
|
A | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00280.hp1 HG00597.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.819+299A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122513 | ||||||
| chr22:30122519
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | NA18942.hp2 NA18951.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+305G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122519 | ||||||
| chr22:30122593
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.819+379G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122593 | ||||||
| chr22:30122610
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819+396A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122610 | ||||||
| chr22:30122720
|
G | A | 32 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0122others(29): Show | 32 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.819+506G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122720 | ||||||
| chr22:30122839
|
G | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 59 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.819+625G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122839 | ||||||
| chr22:30122875
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.819+661A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122875 | ||||||
| chr22:30122892
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.819+678A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30122892 | ||||||
| chr22:30123079
|
T | A | 80 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(77): Show | 80 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.819+865T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123079 | ||||||
| chr22:30123163
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.819+949T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123163 | ||||||
| chr22:30123365
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+1151C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123365 | ||||||
| chr22:30123425
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 242 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.819+1211G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123425 | ||||||
| chr22:30123541
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.819+1327C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123541 | ||||||
| chr22:30123643
|
G | GTATT | 13 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0113others(10): Show | 13 | HG00558.hp2 HG01175.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.819+1464_819+1467d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30123643 | |||||
| chr22:30123643
|
GTATT | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 96 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.819+1464_819+1467d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30123643 | |||||
| chr22:30123643
|
GTATTTAT others(1): Show |
G | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00280.hp1 HG00597.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.819+1460_819+1467d others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30123643 | |||||
| chr22:30123643
|
GTATTTAT others(9): Show |
G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.819+1452_819+1467d others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30123643 | |||||
| chr22:30123836
|
T | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 244 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.819+1622T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123836 | ||||||
| chr22:30123900
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+1686G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123900 | ||||||
| chr22:30123982
|
ATTTC | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+1776_819+1779d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30123982 | |||||
| chr22:30123991
|
T | C | 38 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0085others(35): Show | 38 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+1777T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30123991 | ||||||
| chr22:30124019
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+1805G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124019 | ||||||
| chr22:30124197
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+1983T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124197 | ||||||
| chr22:30124243
|
A | G | 4 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 4 | HG01943.hp1 HG01981.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+2029A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124243 | ||||||
| chr22:30124256
|
A | AAC | 58 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0080others(55): Show | 58 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.819+2078_819+2079d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
A | AACAC | 61 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0075others(58): Show | 61 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.819+2076_819+2079d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
A | AACACAC | 23 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0061others(20): Show | 24 | HG01069.hp1 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+2074_819+2079d others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
A | AACACACA others(1): Show |
40 | a0001c0001t0001g0074a0001c0001t0001g0186a0001c0001t0002g0016others(37): Show | 40 | HG01106.hp1 HG01243.hp1 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.819+2072_819+2079d others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0023others(5): Show | 8 | HG00597.hp2 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.819+2070_819+2079d others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
A | AACACACA others(5): Show |
1 | a0001c0001t0002g0052 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.819+2068_819+2079d others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AAC | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0142a0001c0001t0001g0149others(1): Show | 4 | HG01099.hp1 HG02132.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+2078_819+2079d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACAC | A | 27 | a0001c0001t0001g0060a0001c0001t0001g0123a0001c0001t0001g0124others(24): Show | 27 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.819+2076_819+2079d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACACAC | A | 3 | a0001c0001t0001g0121a0001c0001t0003g0160a0001c0001t0003g0161 | 3 | HG03098.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.819+2074_819+2079d others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACACACA others(1): Show |
A | 4 | a0001c0001t0001g0122a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+2072_819+2079d others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0005 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.819+2070_819+2079d others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACACACA others(5): Show |
A | 57 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0265others(54): Show | 58 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.819+2068_819+2079d others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124256
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0001g0217a0001c0001t0001g0320 | 2 | NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.819+2066_819+2079d others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30124256 | |||||
| chr22:30124294
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.819+2080T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124294 | ||||||
| chr22:30124577
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.819+2363C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124577 | ||||||
| chr22:30124759
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+2545C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124759 | ||||||
| chr22:30124835
|
G | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+2621G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30124835 | ||||||
| chr22:30125019
|
T | C | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.819+2805T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125019 | ||||||
| chr22:30125216
|
C | CT | 42 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0213others(39): Show | 42 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.819+3028dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG02083.hp1 HG03017.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+3021_819+3028d others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0102others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+3020_819+3028d others(11): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0111others(3): Show | 6 | HG01074.hp2 HG01928.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+3019_819+3028d others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0087a0001c0001t0001g0113a0001c0001t0001g0345 | 3 | HG01175.hp2 HG02895.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.819+3018_819+3028d others(13): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0156others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+3017_819+3028d others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(6): Show |
9 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0152others(6): Show | 9 | HG01496.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.819+3016_819+3028d others(15): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(7): Show |
6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG02109.hp2 HG02155.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+3015_819+3028d others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0063a0001c0001t0002g0015a0001c0001t0002g0021others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+3014_819+3028d others(17): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0079a0001c0001t0002g0017a0001c0001t0003g0160others(1): Show | 4 | HG02896.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+3013_819+3028d others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0081a0001c0001t0002g0016a0001c0001t0002g0018 | 3 | HG02630.hp1 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.819+3012_819+3028d others(19): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0099 | 2 | HG02615.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.819+3011_819+3028d others(20): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(12): Show |
5 | a0001c0001t0001g0056a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01884.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+3010_819+3028d others(21): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(13): Show |
15 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0089others(12): Show | 15 | HG00280.hp1 HG01256.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.819+3009_819+3028d others(22): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(14): Show |
11 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0002g0025others(8): Show | 12 | HG00597.hp2 HG01106.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.819+3008_819+3028d others(23): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(15): Show |
10 | a0001c0001t0001g0064a0001c0001t0001g0098a0001c0001t0001g0119others(7): Show | 10 | HG00558.hp1 HG01123.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+3007_819+3028d others(24): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(16): Show |
7 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG02922.hp2 NA18945.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+3006_819+3028d others(25): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(17): Show |
2 | a0001c0001t0002g0028a0001c0001t0002g0039 | 2 | NA18959.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.819+3005_819+3028d others(26): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0093a0001c0001t0002g0046 | 2 | HG03942.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.819+3004_819+3028d others(27): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.819+3003_819+3028d others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0052 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.819+3028_819+3029i others(29): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
CT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0170others(14): Show | 18 | HG02027.hp2 HG02040.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.819+3028delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
CTTTT | C | 28 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0122others(25): Show | 28 | HG00423.hp1 HG00642.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.819+3025_819+3028d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
CTTTTT | C | 20 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0083others(17): Show | 20 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.819+3024_819+3028d others(7): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125216
|
CTTTTTT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+3023_819+3028d others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125216 | |||||
| chr22:30125226
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.819+3012T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125226 | ||||||
| chr22:30125237
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0176 | 3 | HG02040.hp2 NA18747.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.819+3023T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125237 | ||||||
| chr22:30125266
|
CCAG | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.819+3056_819+3058d others(5): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30125266 | |||||
| chr22:30125298
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+3084G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125298 | ||||||
| chr22:30125458
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 59 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.819+3244C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125458 | ||||||
| chr22:30125781
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(57): Show | 61 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.819+3567A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125781 | ||||||
| chr22:30125854
|
G | C | 1 | a0001c0001t0002g0029 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.819+3640G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30125854 | ||||||
| chr22:30126099
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.819+3885T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30126099 | ||||||
| chr22:30126195
|
C | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+3981C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30126195 | ||||||
| chr22:30126224
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.819+4010T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30126224 | ||||||
| chr22:30126424
|
G | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 297 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.819+4210G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30126424 | ||||||
| chr22:30126470
|
T | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(47): Show | 50 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.819+4256T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30126470 | ||||||
| chr22:30127160
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819+4946G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127160 | ||||||
| chr22:30127199
|
C | CT | 92 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0056others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.819+5012dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127199
|
C | CTT | 13 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0098others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.819+5011_819+5012d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127199
|
CT | C | 13 | a0001c0001t0001g0066a0001c0001t0001g0122a0001c0001t0001g0123others(10): Show | 13 | HG01069.hp2 HG01070.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.819+5012delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127199
|
CTTTTTTT | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0266others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.819+5006_819+5012d others(9): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127199
|
CTTTTTTT others(1): Show |
C | 52 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.819+5005_819+5012d others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127199
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+5001_819+5012d others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30127199 | |||||
| chr22:30127220
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.819+5006T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127220 | ||||||
| chr22:30127230
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.819+5016A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127230 | ||||||
| chr22:30127328
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0095others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+5114C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127328 | ||||||
| chr22:30127398
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+5184G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127398 | ||||||
| chr22:30127442
|
C | T | 46 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(43): Show | 46 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.819+5228C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127442 | ||||||
| chr22:30127452
|
C | T | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.819+5238C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127452 | ||||||
| chr22:30127497
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.819+5283A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127497 | ||||||
| chr22:30127509
|
A | C | 1 | a0001c0001t0001g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.819+5295A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127509 | ||||||
| chr22:30127592
|
C | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+5378C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127592 | ||||||
| chr22:30127623
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+5409G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127623 | ||||||
| chr22:30127625
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.819+5411G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127625 | ||||||
| chr22:30127719
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.819+5505A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127719 | ||||||
| chr22:30127848
|
C | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | NA18980.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.819+5634C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127848 | ||||||
| chr22:30127953
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.819+5739C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30127953 | ||||||
| chr22:30128080
|
A | G | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+5866A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128080 | ||||||
| chr22:30128224
|
T | A | 1 | a0001c0001t0002g0059 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.819+6010T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128224 | ||||||
| chr22:30128259
|
C | T | 80 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(77): Show | 80 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.819+6045C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128259 | ||||||
| chr22:30128389
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.819+6175A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128389 | ||||||
| chr22:30128436
|
T | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.819+6222T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128436 | ||||||
| chr22:30128578
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.819+6364C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128578 | ||||||
| chr22:30128721
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+6507T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128721 | ||||||
| chr22:30128772
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.819+6558C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128772 | ||||||
| chr22:30128879
|
A | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.819+6665A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128879 | ||||||
| chr22:30128942
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+6728C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30128942 | ||||||
| chr22:30129035
|
A | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 92 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.819+6821A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129035 | ||||||
| chr22:30129114
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.819+6900A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129114 | ||||||
| chr22:30129173
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0286 | 2 | HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.819+6959G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129173 | ||||||
| chr22:30129217
|
C | CA | 27 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(24): Show | 27 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.819+7042dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAA | 18 | a0001c0001t0001g0003a0001c0001t0001g0165a0001c0001t0001g0214others(15): Show | 19 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.819+7041_819+7042d others(4): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAAAAAA | 9 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG02056.hp2 HG02083.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.819+7037_819+7042d others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAAAAAAA | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0190others(8): Show | 11 | HG02027.hp1 HG02074.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+7036_819+7042d others(9): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.819+7033_819+7042d others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.819+7030_819+7042d others(15): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.819+7029_819+7042d others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.819+7027_819+7042d others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.819+7026_819+7042d others(19): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129217
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0166 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.819+7025_819+7042d others(20): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129217 | |||||
| chr22:30129234
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.819+7022_819+7044d others(25): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129234 | |||||
| chr22:30129235
|
AAAAAAAA others(15): Show |
A | 45 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(42): Show | 45 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.819+7023_819+7044d others(24): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129235 | |||||
| chr22:30129236
|
AAAAAAAA others(14): Show |
A | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.819+7024_819+7044d others(23): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129236 | |||||
| chr22:30129237
|
AAAAAAAA others(13): Show |
A | 25 | a0001c0001t0001g0083a0001c0001t0001g0322a0001c0001t0001g0323others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.819+7025_819+7044d others(22): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129237 | |||||
| chr22:30129238
|
AAAAAAAA others(12): Show |
A | 4 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0332others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+7026_819+7044d others(21): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129238 | |||||
| chr22:30129239
|
AAAAAAAA others(11): Show |
A | 29 | a0001c0001t0001g0066a0001c0001t0001g0123a0001c0001t0001g0124others(26): Show | 29 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.819+7027_819+7044d others(20): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129239 | |||||
| chr22:30129240
|
AAAAAAAA others(10): Show |
A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0130 | 3 | HG02717.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.819+7028_819+7044d others(19): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129240 | |||||
| chr22:30129241
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0035a0001c0001t0002g0053 | 2 | HG02300.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.819+7029_819+7044d others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129241 | |||||
| chr22:30129242
|
AAAAAAAA others(8): Show |
A | 43 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(40): Show | 43 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.819+7030_819+7044d others(17): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129242 | |||||
| chr22:30129243
|
AAAAAAAA others(7): Show |
A | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(22): Show | 26 | HG01884.hp2 HG02129.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.819+7031_819+7044d others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129243 | |||||
| chr22:30129244
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0268a0001c0001t0001g0295others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+7032_819+7044d others(15): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129244 | |||||
| chr22:30129245
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.819+7033_819+7044d others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129245 | |||||
| chr22:30129253
|
AAAAG | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0001t0001g0065others(14): Show | 18 | HG01074.hp2 HG01169.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.819+7041_819+7044d others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129253 | |||||
| chr22:30129254
|
AAAG | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0001g0088others(13): Show | 16 | HG01361.hp2 HG01928.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.819+7042_819+7044d others(5): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30129254 | |||||
| chr22:30129255
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.819+7041A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129255 | ||||||
| chr22:30129474
|
C | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+7260C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129474 | ||||||
| chr22:30129560
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+7346C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129560 | ||||||
| chr22:30129589
|
C | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+7375C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129589 | ||||||
| chr22:30129662
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.819+7448T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129662 | ||||||
| chr22:30129952
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+7738C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129952 | ||||||
| chr22:30129998
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG01884.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.819+7784T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30129998 | ||||||
| chr22:30130020
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+7806T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130020 | ||||||
| chr22:30130450
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+8236C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130450 | ||||||
| chr22:30130586
|
C | CT | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0168others(49): Show | 53 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.819+8394dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30130586 | |||||
| chr22:30130586
|
CT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.819+8394delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30130586 | |||||
| chr22:30130591
|
T | C | 51 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0079others(48): Show | 51 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.819+8377T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130591 | ||||||
| chr22:30130592
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0002g0042 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.819+8378T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130592 | ||||||
| chr22:30130617
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.819+8403G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130617 | ||||||
| chr22:30130643
|
G | T | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(157): Show | 161 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.819+8429G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130643 | ||||||
| chr22:30130680
|
T | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+8466T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130680 | ||||||
| chr22:30130735
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.819+8521G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130735 | ||||||
| chr22:30130952
|
C | T | 5 | a0001c0001t0002g0026a0001c0001t0002g0033a0001c0001t0002g0038others(2): Show | 5 | HG02698.hp1 NA18951.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+8738C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30130952 | ||||||
| chr22:30130990
|
G | GT | 6 | a0001c0001t0001g0136a0001c0001t0001g0190a0001c0001t0001g0283others(3): Show | 6 | HG01192.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+8785dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30130990 | |||||
| chr22:30131472
|
T | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+9258T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30131472 | ||||||
| chr22:30132222
|
T | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+10008T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132222 | ||||||
| chr22:30132232
|
T | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 87 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.819+10018T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132232 | ||||||
| chr22:30132332
|
A | G | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.819+10118A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132332 | ||||||
| chr22:30132451
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.819+10237G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132451 | ||||||
| chr22:30132539
|
C | CA | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 68 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.819+10338dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30132539 | |||||
| chr22:30132553
|
C | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+10339C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132553 | ||||||
| chr22:30132559
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.819+10345C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132559 | ||||||
| chr22:30132841
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.819+10627G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30132841 | ||||||
| chr22:30133000
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.819+10786A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30133000 | ||||||
| chr22:30133466
|
C | CAT | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(165): Show | 169 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.819+11262_819+1126 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30133466 | |||||
| chr22:30133466
|
C | CATAT | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+11260_819+1126 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30133466 | |||||
| chr22:30133466
|
CAT | C | 23 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 23 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.819+11262_819+1126 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30133466 | |||||
| chr22:30133636
|
T | TA | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01099.hp1 HG01192.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+11427dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30133636 | |||||
| chr22:30133641
|
AC | A | 4 | a0001c0001t0001g0264a0001c0001t0003g0160a0001c0001t0003g0161others(1): Show | 4 | HG03098.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+11428delC | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30133641 | ||||||
| chr22:30133642
|
C | A | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(188): Show | 192 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.819+11428C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30133642 | ||||||
| chr22:30133649
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0191 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.819+11436_819+1144 others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30133649 | |||||
| chr22:30133752
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0079others(53): Show | 57 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.819+11538G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30133752 | ||||||
| chr22:30133971
|
T | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.819+11757T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30133971 | ||||||
| chr22:30134136
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 298 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.819+11922T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30134136 | ||||||
| chr22:30134243
|
C | CA | 38 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(35): Show | 38 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+12035dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30134243 | |||||
| chr22:30134339
|
C | T | 38 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(35): Show | 38 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+12125C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30134339 | ||||||
| chr22:30134368
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.819+12154C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30134368 | ||||||
| chr22:30134387
|
T | TTA | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+12184_819+1218 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30134387 | |||||
| chr22:30134387
|
TTA | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+12184_819+1218 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30134387 | |||||
| chr22:30134580
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.819+12366C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30134580 | ||||||
| chr22:30134701
|
GA | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.819+12496delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30134701 | |||||
| chr22:30135015
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.819+12801A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135015 | ||||||
| chr22:30135102
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 245 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.819+12888C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135102 | ||||||
| chr22:30135112
|
CAT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.819+12903_819+1290 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30135112 | |||||
| chr22:30135360
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13146C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135360 | ||||||
| chr22:30135363
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13149G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135363 | ||||||
| chr22:30135368
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13154G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135368 | ||||||
| chr22:30135369
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13155A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135369 | ||||||
| chr22:30135370
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13156G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135370 | ||||||
| chr22:30135373
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13159A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135373 | ||||||
| chr22:30135374
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13160C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135374 | ||||||
| chr22:30135375
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13161C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135375 | ||||||
| chr22:30135388
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.819+13174G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135388 | ||||||
| chr22:30135389
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+13175G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135389 | ||||||
| chr22:30135436
|
G | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+13222G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135436 | ||||||
| chr22:30135490
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.819+13276A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30135490 | ||||||
| chr22:30136033
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+13819T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136033 | ||||||
| chr22:30136063
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819+13849C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136063 | ||||||
| chr22:30136068
|
A | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+13854A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136068 | ||||||
| chr22:30136104
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.819+13890A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136104 | ||||||
| chr22:30136264
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.819+14050C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136264 | ||||||
| chr22:30136617
|
C | CTT | 31 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0122others(28): Show | 31 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.819+14413_819+1441 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30136617 | |||||
| chr22:30136617
|
CT | C | 14 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+14414delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30136617 | |||||
| chr22:30136620
|
T | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+14406T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136620 | ||||||
| chr22:30136628
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+14414T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136628 | ||||||
| chr22:30136682
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.819+14468T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136682 | ||||||
| chr22:30136684
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.819+14470C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30136684 | ||||||
| chr22:30137076
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 244 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.819+14862A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137076 | ||||||
| chr22:30137084
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.819+14870G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137084 | ||||||
| chr22:30137130
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.819+14916G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137130 | ||||||
| chr22:30137196
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.819+14982C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137196 | ||||||
| chr22:30137289
|
T | G | 5 | a0002c0002t0001g0054a0002c0002t0001g0070a0002c0002t0001g0071others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+15075T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137289 | ||||||
| chr22:30137396
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.819+15182C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137396 | ||||||
| chr22:30137420
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.819+15206A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137420 | ||||||
| chr22:30137551
|
CAGAG | C | 6 | a0001c0001t0001g0264a0001c0001t0003g0160a0001c0001t0003g0161others(3): Show | 6 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+15341_819+1534 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30137551 | |||||
| chr22:30137788
|
G | T | 1 | a0001c0001t0002g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.819+15574G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137788 | ||||||
| chr22:30137837
|
C | A | 31 | a0001c0001t0001g0066a0001c0001t0001g0122a0001c0001t0001g0123others(28): Show | 31 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.819+15623C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137837 | ||||||
| chr22:30137940
|
A | G | 80 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(77): Show | 80 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.819+15726A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30137940 | ||||||
| chr22:30138150
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.819+15936C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30138150 | ||||||
| chr22:30138172
|
G | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.819+15958G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30138172 | ||||||
| chr22:30138243
|
A | AT | 70 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(67): Show | 70 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.819+16043dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30138243 | |||||
| chr22:30138243
|
A | ATT | 10 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0285others(7): Show | 10 | HG01175.hp1 HG02258.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.819+16042_819+1604 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30138243 | |||||
| chr22:30138318
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.819+16104G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30138318 | ||||||
| chr22:30138364
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+16150C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30138364 | ||||||
| chr22:30138770
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG01884.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.819+16556A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30138770 | ||||||
| chr22:30139254
|
C | CTA | 42 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0065others(39): Show | 42 | HG00280.hp1 HG00438.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.819+17072_819+1707 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATA | 43 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0056others(40): Show | 44 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.819+17070_819+1707 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATA | 32 | a0001c0001t0001g0014a0001c0001t0001g0075a0001c0001t0001g0125others(29): Show | 32 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.819+17068_819+1707 others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(1): Show |
39 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 40 | HG00558.hp2 HG01099.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.819+17066_819+1707 others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(3): Show |
29 | a0001c0001t0001g0060a0001c0001t0001g0123a0001c0001t0001g0129others(26): Show | 29 | HG00280.hp2 HG00673.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.819+17064_819+1707 others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(5): Show |
20 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0145others(17): Show | 20 | HG01243.hp2 HG02055.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.819+17062_819+1707 others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(7): Show |
6 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0171others(3): Show | 6 | HG02965.hp2 NA18522.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+17060_819+1707 others(18): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(9): Show |
6 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0308others(3): Show | 6 | HG02040.hp1 HG02155.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+17058_819+1707 others(20): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.819+17056_819+1707 others(22): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
CTA | C | 37 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0104others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.819+17072_819+1707 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
CTATA | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0099others(11): Show | 15 | HG00558.hp1 HG01175.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.819+17070_819+1707 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
CTATATA | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0260a0001c0001t0001g0262others(2): Show | 5 | HG01192.hp2 HG01433.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+17068_819+1707 others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
CTATATAT others(3): Show |
C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+17064_819+1707 others(14): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139254
|
CTATATAT others(5): Show |
C | 9 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 9 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.819+17062_819+1707 others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139254 | |||||
| chr22:30139266
|
A | C | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819+17052A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30139266 | ||||||
| chr22:30139273
|
T | G | 1 | a0001c0001t0001g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.819+17059T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30139273 | ||||||
| chr22:30139324
|
T | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+17110T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30139324 | ||||||
| chr22:30139580
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0095others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+17366G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30139580 | ||||||
| chr22:30139743
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.819+17529A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30139743 | ||||||
| chr22:30139955
|
C | CTG | 34 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0100others(31): Show | 34 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.819+17759_819+1776 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139955 | |||||
| chr22:30139955
|
C | CTGTG | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 61 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.819+17757_819+1776 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30139955 | |||||
| chr22:30140067
|
T | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(39): Show | 43 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.819+17853T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30140067 | ||||||
| chr22:30140102
|
A | G | 24 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0089others(21): Show | 24 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+17888A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30140102 | ||||||
| chr22:30140114
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.819+17900A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30140114 | ||||||
| chr22:30140276
|
GA | G | 32 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0122others(29): Show | 32 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.819+18067delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30140276 | |||||
| chr22:30140386
|
G | A | 1 | a0001c0001t0001g0004 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.819+18172G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30140386 | ||||||
| chr22:30140548
|
CTAAGT | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+18337_819+1834 others(9): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30140548 | |||||
| chr22:30141029
|
T | TCTCTGTC others(590): Show |
1 | a0001c0001t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.819+18844_819+1944 others(601): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30141029 | |||||
| chr22:30141279
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819+19065T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141279 | ||||||
| chr22:30141348
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0254 | 3 | HG00642.hp2 HG01074.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.819+19134T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141348 | ||||||
| chr22:30141494
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.819+19280G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141494 | ||||||
| chr22:30141537
|
T | C | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 195 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.819+19323T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141537 | ||||||
| chr22:30141595
|
CT | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 102 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.819+19398delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30141595 | |||||
| chr22:30141795
|
C | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+19581C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141795 | ||||||
| chr22:30141829
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.819+19615C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141829 | ||||||
| chr22:30141886
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.819+19672C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30141886 | ||||||
| chr22:30142344
|
C | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0237 | 3 | HG00741.hp1 HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.819+20130C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30142344 | ||||||
| chr22:30142355
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.819+20141G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30142355 | ||||||
| chr22:30142409
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.819+20195T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30142409 | ||||||
| chr22:30142664
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.819+20450A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30142664 | ||||||
| chr22:30142888
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0052 | 3 | HG02523.hp2 NA18962.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.819+20674A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30142888 | ||||||
| chr22:30143187
|
GTTTA | G | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG00642.hp1 HG01070.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+20978_819+2098 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30143187 | |||||
| chr22:30143286
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0074others(8): Show | 11 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+21072C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30143286 | ||||||
| chr22:30143414
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819+21200T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30143414 | ||||||
| chr22:30143438
|
T | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(57): Show | 61 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.819+21224T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30143438 | ||||||
| chr22:30143832
|
C | T | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(160): Show | 164 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.819+21618C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30143832 | ||||||
| chr22:30143874
|
G | T | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819+21660G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30143874 | ||||||
| chr22:30144021
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.819+21807A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144021 | ||||||
| chr22:30144299
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.819+22085C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144299 | ||||||
| chr22:30144408
|
T | G | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+22194T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144408 | ||||||
| chr22:30144417
|
A | G | 23 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 23 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.819+22203A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144417 | ||||||
| chr22:30144513
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.819+22299A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144513 | ||||||
| chr22:30144601
|
T | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.819+22387T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144601 | ||||||
| chr22:30144635
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+22421G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144635 | ||||||
| chr22:30144794
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.819+22580T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144794 | ||||||
| chr22:30144810
|
TCCATCTC others(1): Show |
T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+22601_819+2260 others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30144810 | |||||
| chr22:30144878
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0283others(1): Show | 4 | NA18943.hp2 NA18952.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+22664G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144878 | ||||||
| chr22:30144913
|
G | T | 1 | a0001c0001t0004g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.819+22699G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144913 | ||||||
| chr22:30144945
|
G | A | 38 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(35): Show | 38 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+22731G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30144945 | ||||||
| chr22:30145100
|
A | G | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+22886A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145100 | ||||||
| chr22:30145109
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.819+22895T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145109 | ||||||
| chr22:30145254
|
A | C | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.819+23040A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145254 | ||||||
| chr22:30145470
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.819+23256T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145470 | ||||||
| chr22:30145635
|
G | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01192.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+23421G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145635 | ||||||
| chr22:30145681
|
G | A | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.819+23467G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145681 | ||||||
| chr22:30145811
|
A | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0013a0004c0003t0001g0008 | 3 | HG02622.hp1 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.819+23597A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30145811 | ||||||
| chr22:30146003
|
C | G | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.819+23789C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146003 | ||||||
| chr22:30146168
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 245 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.819+23954T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146168 | ||||||
| chr22:30146217
|
G | A | 5 | a0001c0001t0001g0301a0001c0001t0001g0303a0001c0001t0001g0304others(2): Show | 5 | NA18612.hp2 NA18949.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+24003G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146217 | ||||||
| chr22:30146443
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+24229C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146443 | ||||||
| chr22:30146691
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0267a0001c0001t0001g0287others(3): Show | 6 | HG00438.hp1 NA18956.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+24477C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146691 | ||||||
| chr22:30146809
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.819+24595A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30146809 | ||||||
| chr22:30147067
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+24853C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147067 | ||||||
| chr22:30147371
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.819+25157G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147371 | ||||||
| chr22:30147373
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.819+25159G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147373 | ||||||
| chr22:30147418
|
GA | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+25213delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30147418 | |||||
| chr22:30147427
|
A | G | 4 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 4 | HG01943.hp1 HG01981.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+25213A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147427 | ||||||
| chr22:30147514
|
T | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.819+25300T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147514 | ||||||
| chr22:30147528
|
A | C | 1 | a0001c0001t0002g0052 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.819+25314A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147528 | ||||||
| chr22:30147835
|
C | T | 80 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(77): Show | 80 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.819+25621C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147835 | ||||||
| chr22:30147845
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+25631C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147845 | ||||||
| chr22:30147985
|
C | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.819+25771C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30147985 | ||||||
| chr22:30148089
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.819+25875C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148089 | ||||||
| chr22:30148527
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 243 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.819+26313G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148527 | ||||||
| chr22:30148570
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.819+26356T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148570 | ||||||
| chr22:30148775
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.819+26561C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148775 | ||||||
| chr22:30148832
|
G | A | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.819+26618G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148832 | ||||||
| chr22:30148865
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.819+26651C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148865 | ||||||
| chr22:30148900
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.819+26686G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148900 | ||||||
| chr22:30148965
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.819+26751C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148965 | ||||||
| chr22:30148973
|
C | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | NA18612.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.819+26759C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148973 | ||||||
| chr22:30148979
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.819+26765G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30148979 | ||||||
| chr22:30149160
|
A | G | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.820-26903A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30149160 | ||||||
| chr22:30149403
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-26660A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30149403 | ||||||
| chr22:30149637
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.820-26426C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30149637 | ||||||
| chr22:30149991
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-26072G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30149991 | ||||||
| chr22:30150154
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.820-25909G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150154 | ||||||
| chr22:30150256
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.820-25807C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150256 | ||||||
| chr22:30150383
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.820-25680C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150383 | ||||||
| chr22:30150386
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-25677G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150386 | ||||||
| chr22:30150484
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG00642.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.820-25579C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150484 | ||||||
| chr22:30150486
|
C | CCTCTTCC others(24): Show |
1 | a0001c0001t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.820-25573_820-2554 others(35): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30150486 | |||||
| chr22:30150557
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.820-25506T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150557 | ||||||
| chr22:30150664
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.820-25399G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150664 | ||||||
| chr22:30150779
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.820-25284C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30150779 | ||||||
| chr22:30151133
|
T | A | 1 | a0001c0001t0002g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.820-24930T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151133 | ||||||
| chr22:30151314
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.820-24749T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151314 | ||||||
| chr22:30151379
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-24684A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151379 | ||||||
| chr22:30151407
|
A | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-24656A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151407 | ||||||
| chr22:30151756
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.820-24307A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151756 | ||||||
| chr22:30151821
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.820-24242C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30151821 | ||||||
| chr22:30152135
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.820-23928A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152135 | ||||||
| chr22:30152301
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-23762A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152301 | ||||||
| chr22:30152397
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.820-23666G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152397 | ||||||
| chr22:30152633
|
G | A | 32 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0122others(29): Show | 32 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.820-23430G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152633 | ||||||
| chr22:30152874
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.820-23189G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152874 | ||||||
| chr22:30152950
|
C | T | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.820-23113C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30152950 | ||||||
| chr22:30153024
|
T | G | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-23039T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153024 | ||||||
| chr22:30153043
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-23020T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153043 | ||||||
| chr22:30153080
|
C | G | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-22983C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153080 | ||||||
| chr22:30153081
|
CAT | C | 31 | a0001c0001t0001g0066a0001c0001t0001g0122a0001c0001t0001g0123others(28): Show | 31 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.820-22981_820-2298 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153081 | ||||||
| chr22:30153082
|
A | C | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(192): Show | 196 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.820-22981A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153082 | ||||||
| chr22:30153524
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.820-22539C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153524 | ||||||
| chr22:30153578
|
G | A | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-22485G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153578 | ||||||
| chr22:30153613
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820-22450A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153613 | ||||||
| chr22:30153618
|
T | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-22445T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153618 | ||||||
| chr22:30153734
|
TC | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-22328delC | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153734 | ||||||
| chr22:30153775
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-22288T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153775 | ||||||
| chr22:30153922
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.820-22141A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30153922 | ||||||
| chr22:30154021
|
A | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.820-22042A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154021 | ||||||
| chr22:30154085
|
C | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-21978C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154085 | ||||||
| chr22:30154203
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.820-21860C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154203 | ||||||
| chr22:30154391
|
C | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-21672C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154391 | ||||||
| chr22:30154876
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-21187C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154876 | ||||||
| chr22:30154941
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(57): Show | 61 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-21122G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30154941 | ||||||
| chr22:30155076
|
T | A | 2 | a0001c0001t0001g0319a0001c0001t0002g0019 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.820-20987T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155076 | ||||||
| chr22:30155076
|
T | TA | 12 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0088others(9): Show | 12 | HG02451.hp2 HG04204.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.820-20971dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30155076 | |||||
| chr22:30155076
|
TA | T | 23 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0074others(20): Show | 23 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.820-20971delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30155076 | |||||
| chr22:30155077
|
A | T | 29 | a0001c0001t0001g0060a0001c0001t0001g0121a0001c0001t0001g0122others(26): Show | 29 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.820-20986A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155077 | ||||||
| chr22:30155078
|
A | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0123a0001c0001t0001g0145others(2): Show | 5 | HG01099.hp1 HG02040.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-20985A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155078 | ||||||
| chr22:30155089
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.820-20974A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155089 | ||||||
| chr22:30155404
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.820-20659G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155404 | ||||||
| chr22:30155528
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-20535G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155528 | ||||||
| chr22:30155655
|
A | AAC | 13 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(10): Show | 13 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.820-20390_820-2038 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30155655 | |||||
| chr22:30155856
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.820-20207T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30155856 | ||||||
| chr22:30156024
|
AG | A | 37 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(34): Show | 37 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.820-20037delG | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30156024 | |||||
| chr22:30156154
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-19909G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30156154 | ||||||
| chr22:30156312
|
TTC | T | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-19749_820-1974 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30156312 | |||||
| chr22:30156522
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 245 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.820-19541G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30156522 | ||||||
| chr22:30156706
|
A | G | 103 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(100): Show | 103 | HG00280.hp1 HG00597.hp2 HG01069.hp1 others(100): Show |
intron_variant | MODIFIER | c.820-19357A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30156706 | ||||||
| chr22:30156824
|
A | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-19239A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30156824 | ||||||
| chr22:30156885
|
A | G | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0258 | 3 | HG02109.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.820-19178A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30156885 | ||||||
| chr22:30157106
|
T | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-18957T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30157106 | ||||||
| chr22:30157209
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.820-18854A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30157209 | ||||||
| chr22:30157220
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.820-18843G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30157220 | ||||||
| chr22:30157730
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-18333T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30157730 | ||||||
| chr22:30157812
|
C | A | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-18251C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30157812 | ||||||
| chr22:30158080
|
G | GA | 55 | a0001c0001t0001g0007a0001c0001t0001g0079a0001c0001t0001g0080others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.820-17974dupA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158080 | |||||
| chr22:30158215
|
A | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.820-17848A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158215 | ||||||
| chr22:30158220
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-17843C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158220 | ||||||
| chr22:30158357
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.820-17706T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158357 | ||||||
| chr22:30158473
|
CTTTTCTT others(5): Show |
C | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-17576_820-1756 others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158473 | |||||
| chr22:30158503
|
CCTT | C | 7 | a0001c0001t0001g0322a0001c0001t0001g0325a0001c0001t0001g0330others(4): Show | 7 | HG02109.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-17556_820-1755 others(7): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158503 | |||||
| chr22:30158551
|
TCCCTC | T | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-17499_820-1749 others(9): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158551 | |||||
| chr22:30158555
|
T | TC | 13 | a0001c0001t0001g0177a0001c0001t0001g0265a0001c0001t0001g0266others(10): Show | 13 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.820-17504dupC | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158555 | |||||
| chr22:30158560
|
T | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(43): Show | 46 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.820-17503T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158560 | ||||||
| chr22:30158564
|
C | T | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 63 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.820-17499C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158564 | ||||||
| chr22:30158565
|
T | TC | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 63 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.820-17495dupC | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158565 | |||||
| chr22:30158573
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-17490C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158573 | ||||||
| chr22:30158578
|
C | CTT | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-17485_820-1748 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158578 | ||||||
| chr22:30158578
|
C | T | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-17485C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158578 | ||||||
| chr22:30158583
|
C | CCT | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.820-17480_820-1747 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158583 | ||||||
| chr22:30158583
|
C | CTCCTTCC others(1): Show |
148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 150 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.820-17472_820-1746 others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158583 | |||||
| chr22:30158587
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-17476T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158587 | ||||||
| chr22:30158591
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-17472T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158591 | ||||||
| chr22:30158594
|
C | CCTCCCTC others(5): Show |
59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-17469_820-1746 others(16): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158594 | ||||||
| chr22:30158594
|
C | CCTTT | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-17469_820-1746 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158594 | ||||||
| chr22:30158595
|
T | G | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 63 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.820-17468T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158595 | ||||||
| chr22:30158595
|
T | TTCCCTCC others(9): Show |
25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-17455_820-1745 others(20): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158595 | |||||
| chr22:30158595
|
T | TTCCTTCC others(17): Show |
5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-17465_820-1746 others(28): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158595 | |||||
| chr22:30158599
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.820-17464C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158599 | ||||||
| chr22:30158604
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.820-17459T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158604 | ||||||
| chr22:30158611
|
G | GTCCCTCC others(1): Show |
53 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(50): Show | 53 | HG00597.hp2 HG01106.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.820-17442_820-1743 others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30158611 | |||||
| chr22:30158614
|
C | T | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0243others(3): Show | 6 | NA18968.hp1 NA18977.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-17449C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158614 | ||||||
| chr22:30158629
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820-17434T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158629 | ||||||
| chr22:30158784
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.820-17279C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30158784 | ||||||
| chr22:30159227
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(47): Show | 50 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.820-16836G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30159227 | ||||||
| chr22:30159911
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.820-16152C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30159911 | ||||||
| chr22:30159942
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-16121G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30159942 | ||||||
| chr22:30160061
|
A | G | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.820-16002A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160061 | ||||||
| chr22:30160112
|
G | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.820-15951G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160112 | ||||||
| chr22:30160200
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.820-15863A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160200 | ||||||
| chr22:30160659
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.820-15404C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160659 | ||||||
| chr22:30160697
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.820-15366G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160697 | ||||||
| chr22:30160711
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.820-15352A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160711 | ||||||
| chr22:30160730
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.820-15333C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160730 | ||||||
| chr22:30160856
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.820-15207T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160856 | ||||||
| chr22:30160999
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.820-15064T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30160999 | ||||||
| chr22:30161183
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.820-14880A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161183 | ||||||
| chr22:30161278
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0235a0001c0001t0001g0238 | 4 | HG01106.hp2 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-14785G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161278 | ||||||
| chr22:30161289
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0066others(39): Show | 43 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.820-14774T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161289 | ||||||
| chr22:30161292
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.820-14771C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161292 | ||||||
| chr22:30161317
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.820-14746T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161317 | ||||||
| chr22:30161655
|
T | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.820-14408T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161655 | ||||||
| chr22:30161908
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.820-14155T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161908 | ||||||
| chr22:30161950
|
G | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.820-14113G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30161950 | ||||||
| chr22:30162107
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-13956G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162107 | ||||||
| chr22:30162177
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.820-13886G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162177 | ||||||
| chr22:30162239
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.820-13824G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162239 | ||||||
| chr22:30162271
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.820-13792A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162271 | ||||||
| chr22:30162318
|
T | TAC | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02027.hp1 HG02040.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.820-13714_820-1371 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162318 | |||||
| chr22:30162318
|
T | TACAC | 37 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(34): Show | 38 | HG00558.hp1 HG01074.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.820-13716_820-1371 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162318 | |||||
| chr22:30162318
|
TACAC | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.820-13716_820-1371 others(8): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162318 | |||||
| chr22:30162318
|
TACACAC | T | 132 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.820-13718_820-1371 others(10): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162318 | |||||
| chr22:30162318
|
TACACACA others(1): Show |
T | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0066others(50): Show | 54 | HG00423.hp1 HG00642.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.820-13720_820-1371 others(12): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162318 | |||||
| chr22:30162507
|
C | T | 33 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0121others(30): Show | 33 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.820-13556C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162507 | ||||||
| chr22:30162510
|
A | G | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.820-13553A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162510 | ||||||
| chr22:30162660
|
G | C | 1 | a0001c0001t0001g0183 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.820-13403G>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162660 | ||||||
| chr22:30162670
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.820-13393A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162670 | ||||||
| chr22:30162701
|
C | CT | 6 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0110others(3): Show | 6 | HG01192.hp1 HG03669.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-13343dupT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162701 | |||||
| chr22:30162701
|
CT | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(105): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.820-13343delT | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30162701 | |||||
| chr22:30162771
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820-13292C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162771 | ||||||
| chr22:30162846
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-13217G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30162846 | ||||||
| chr22:30163005
|
T | A | 9 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(6): Show | 9 | HG00639.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.820-13058T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30163005 | ||||||
| chr22:30163077
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-12986G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30163077 | ||||||
| chr22:30163255
|
CTT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-12806_820-1280 others(6): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30163255 | |||||
| chr22:30163329
|
T | A | 18 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 18 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.820-12734T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30163329 | ||||||
| chr22:30163691
|
A | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.820-12372A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30163691 | ||||||
| chr22:30163845
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.820-12218G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30163845 | ||||||
| chr22:30164017
|
T | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.820-12046T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164017 | ||||||
| chr22:30164165
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.820-11898T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164165 | ||||||
| chr22:30164581
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.820-11482G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164581 | ||||||
| chr22:30164684
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-11379G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164684 | ||||||
| chr22:30164696
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820-11367G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164696 | ||||||
| chr22:30164909
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.820-11154C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30164909 | ||||||
| chr22:30165521
|
C | A | 1 | a0001c0001t0001g0343 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.820-10542C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30165521 | ||||||
| chr22:30165753
|
A | G | 38 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(35): Show | 38 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.820-10310A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30165753 | ||||||
| chr22:30165922
|
A | C | 1 | a0001c0001t0001g0326 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.820-10141A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30165922 | ||||||
| chr22:30165960
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.820-10103T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30165960 | ||||||
| chr22:30165985
|
ATTC | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-10069_820-1006 others(7): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30165985 | |||||
| chr22:30166240
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.820-9823C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166240 | ||||||
| chr22:30166250
|
C | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(47): Show | 50 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.820-9813C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166250 | ||||||
| chr22:30166395
|
A | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0066others(39): Show | 43 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.820-9668A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166395 | ||||||
| chr22:30166497
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.820-9566T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166497 | ||||||
| chr22:30166655
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.820-9408T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166655 | ||||||
| chr22:30166875
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18945.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.820-9188T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166875 | ||||||
| chr22:30166998
|
A | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(43): Show | 46 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.820-9065A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30166998 | ||||||
| chr22:30167036
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.820-9027A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167036 | ||||||
| chr22:30167189
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820-8874C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167189 | ||||||
| chr22:30167231
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0301others(7): Show | 11 | HG02129.hp1 HG04204.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.820-8832T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167231 | ||||||
| chr22:30167312
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(51): Show | 54 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.820-8751C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167312 | ||||||
| chr22:30167354
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-8709G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167354 | ||||||
| chr22:30167394
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-8669T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167394 | ||||||
| chr22:30167461
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820-8602T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167461 | ||||||
| chr22:30167725
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG00642.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.820-8338A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167725 | ||||||
| chr22:30167731
|
A | T | 45 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(42): Show | 45 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.820-8332A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30167731 | ||||||
| chr22:30168060
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.820-8003T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168060 | ||||||
| chr22:30168092
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18945.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.820-7971C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168092 | ||||||
| chr22:30168112
|
T | A | 1 | a0001c0001t0002g0052 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.820-7951T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168112 | ||||||
| chr22:30168175
|
A | T | 25 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(22): Show | 25 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.820-7888A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168175 | ||||||
| chr22:30168182
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01081.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.820-7881T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168182 | ||||||
| chr22:30168234
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.820-7829A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168234 | ||||||
| chr22:30168413
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-7650G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168413 | ||||||
| chr22:30168631
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.820-7432C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168631 | ||||||
| chr22:30168892
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-7171C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30168892 | ||||||
| chr22:30169003
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18945.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.820-7060T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169003 | ||||||
| chr22:30169188
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820-6875A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169188 | ||||||
| chr22:30169326
|
C | T | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-6737C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169326 | ||||||
| chr22:30169505
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.820-6558T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169505 | ||||||
| chr22:30169644
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02132.hp2 NA18946.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-6419C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169644 | ||||||
| chr22:30169710
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.820-6353C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169710 | ||||||
| chr22:30169711
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-6352G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169711 | ||||||
| chr22:30169819
|
C | G | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.820-6244C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169819 | ||||||
| chr22:30169984
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-6079G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30169984 | ||||||
| chr22:30170136
|
C | T | 5 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0202others(2): Show | 5 | HG00673.hp2 HG02074.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-5927C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170136 | ||||||
| chr22:30170303
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820-5760C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170303 | ||||||
| chr22:30170380
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.820-5683C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170380 | ||||||
| chr22:30170458
|
C | A | 1 | a0002c0002t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-5605C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170458 | ||||||
| chr22:30170545
|
A | T | 2 | a0001c0001t0004g0158a0001c0001t0004g0159 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.820-5518A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170545 | ||||||
| chr22:30170582
|
T | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00423.hp1 HG01981.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.820-5481T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170582 | ||||||
| chr22:30170668
|
C | G | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-5395C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170668 | ||||||
| chr22:30170705
|
G | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 88 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.820-5358G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170705 | ||||||
| chr22:30170744
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.820-5319G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170744 | ||||||
| chr22:30170970
|
A | G | 14 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0285others(11): Show | 14 | HG00639.hp1 HG01175.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.820-5093A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30170970 | ||||||
| chr22:30171207
|
T | C | 23 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 23 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.820-4856T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171207 | ||||||
| chr22:30171242
|
C | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.820-4821C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171242 | ||||||
| chr22:30171701
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.820-4362T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171701 | ||||||
| chr22:30171741
|
A | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0066others(39): Show | 43 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.820-4322A>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171741 | ||||||
| chr22:30171918
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0163others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.820-4145C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171918 | ||||||
| chr22:30171969
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-4094G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171969 | ||||||
| chr22:30171992
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-4071T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30171992 | ||||||
| chr22:30172225
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.820-3838G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30172225 | ||||||
| chr22:30172285
|
C | G | 1 | a0003c0004t0001g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.820-3778C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30172285 | ||||||
| chr22:30172640
|
C | A | 1 | a0001c0001t0004g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-3423C>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30172640 | ||||||
| chr22:30172749
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0163others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.820-3314G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30172749 | ||||||
| chr22:30172887
|
CA | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0196others(4): Show | 7 | HG01943.hp1 HG02523.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-3162delA | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30172887 | |||||
| chr22:30172902
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.820-3161T>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30172902 | ||||||
| chr22:30173011
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.820-3052G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30173011 | ||||||
| chr22:30173848
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.820-2215G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30173848 | ||||||
| chr22:30173902
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00280.hp1 HG00597.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.820-2161A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30173902 | ||||||
| chr22:30173941
|
T | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0333a0001c0001t0001g0336 | 3 | HG02055.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.820-2122T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30173941 | ||||||
| chr22:30174033
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 154 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.820-2030A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174033 | ||||||
| chr22:30174038
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.820-2025G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174038 | ||||||
| chr22:30174303
|
G | A | 26 | a0001c0001t0001g0083a0001c0001t0001g0322a0001c0001t0001g0323others(23): Show | 26 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.820-1760G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174303 | ||||||
| chr22:30174419
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.820-1644A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174419 | ||||||
| chr22:30174442
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.820-1621A>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174442 | ||||||
| chr22:30174454
|
C | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0266others(45): Show | 48 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-1609C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174454 | ||||||
| chr22:30174562
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1501G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174562 | ||||||
| chr22:30174804
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.820-1259C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174804 | ||||||
| chr22:30174890
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1173C>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174890 | ||||||
| chr22:30174891
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.820-1172G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30174891 | ||||||
| chr22:30175043
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.820-1020G>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175043 | ||||||
| chr22:30175109
|
G | A | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.820-954G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175109 | ||||||
| chr22:30175121
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.820-942T>C | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175121 | ||||||
| chr22:30175237
|
T | TTATATAT others(23): Show |
47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(44): Show | 48 | HG00558.hp1 HG01074.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.820-823_820-794dup others(30): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175237 | |||||
| chr22:30175237
|
T | TTATATAT others(26): Show |
148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 150 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.820-774_820-742dup others(33): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175237 | |||||
| chr22:30175237
|
T | TTATATAT others(59): Show |
1 | a0001c0001t0001g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.820-807_820-742dup others(66): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175237 | |||||
| chr22:30175237
|
TTATATAT others(26): Show |
T | 3 | a0002c0002t0001g0054a0002c0002t0001g0070a0002c0002t0001g0071 | 3 | HG01243.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.820-774_820-742del others(33): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175237 | |||||
| chr22:30175250
|
A | T | 1 | a0002c0002t0001g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.820-813A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175250 | ||||||
| chr22:30175283
|
A | T | 3 | a0002c0002t0001g0054a0002c0002t0001g0070a0002c0002t0001g0071 | 3 | HG01243.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.820-780A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175283 | ||||||
| chr22:30175283
|
AATATAGA others(25): Show |
A | 1 | a0002c0002t0001g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.820-778_820-747del others(32): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175283 | |||||
| chr22:30175316
|
A | AAT | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 8 | HG02083.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-730_820-729dup others(2): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175316 | |||||
| chr22:30175316
|
A | AATATAGA others(28): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0164a0001c0001t0001g0173others(7): Show | 11 | HG00280.hp2 HG01069.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.820-742_820-741ins others(35): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175316 | |||||
| chr22:30175316
|
A | T | 2 | a0001c0001t0004g0159a0002c0002t0001g0072 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.820-747A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175316 | ||||||
| chr22:30175318
|
T | TATAGAAT others(55): Show |
1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.820-742_820-741ins others(62): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175318 | |||||
| chr22:30175318
|
T | TATAGAAT others(24): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0182a0001c0001t0001g0200 | 3 | HG01192.hp1 HG02083.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.820-742_820-741ins others(31): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175318 | |||||
| chr22:30175318
|
T | TATAGAAT others(57): Show |
30 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0123others(27): Show | 30 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.820-742_820-741ins others(64): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175318 | |||||
| chr22:30175318
|
T | TATAGAAT others(90): Show |
1 | a0001c0001t0001g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.820-742_820-741ins others(97): Show |
HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr22 | 30175318 | |||||
| chr22:30175466
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-597G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175466 | ||||||
| chr22:30175862
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.820-201C>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175862 | ||||||
| chr22:30175950
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.820-113T>G | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30175950 | ||||||
| chr22:30176013
|
A | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00558.hp1 NA18962.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-50A>T | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30176013 | ||||||
| chr22:30176049
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.820-14G>A | HORMAD2 | ENSG00000176635.18 | transcript | ENST00000336726.11 | protein_coding | 10/10 | chr22 | 30176049 |