Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54870 |
|---|---|
| ensemblid | ENSG00000198218.12 |
| hgncid | 24713 |
| symbol | QRICH1 |
| name | glutamine rich 1 |
| refseq_nuc | NM_198880.3 |
| refseq_prot | NP_942581.1 |
| ensembl_nuc | ENST00000395443.7 |
| ensembl_prot | ENSP00000378830.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49029707 |
| end | 49094071 |
| strand | - |
| ver | v1.2 |
| region | chr3:49029707-49094071 |
| region5000 | chr3:49024707-49099071 |
| regionname0 | QRICH1_chr3_49029707_49094071 |
| regionname5000 | QRICH1_chr3_49024707_49099071 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 776 | 206 | 78 | 40 | 51 | 11 | 24 | 34 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0002 | 0/0 | 776 | 20 | 0 | 6 | 9 | 3 | 2 | 6 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2331 | 204 | 77 | 40 | 50 | 11 | 24 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| c0002 | 0/0 | 2331 | 20 | 0 | 6 | 9 | 3 | 2 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| c0003 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| c0004 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 927 | 211 | 72 | 44 | 54 | 14 | 25 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0002 | 0/0 | 928 | 5 | 4 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0003 | 0/0 | 930 | 3 | 2 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0004 | 0/0 | 927 | 3 | 0 | 0 | 3 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0005 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0006 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0007 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| t0008 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2331 | 204 | 77 | 40 | 50 | 11 | 24 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0003 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0004 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0002c0002 | 0/0 | 2331 | 20 | 0 | 6 | 9 | 3 | 2 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3257 | 194 | 72 | 38 | 48 | 11 | 23 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0002 | 0/0 | 3258 | 4 | 3 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0003 | 0/0 | 3260 | 2 | 2 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0005 | 0/0 | 3257 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0006 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0007 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0001t0008 | 0/0 | 3257 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0003t0001 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0001c0004t0002 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0002c0002t0001 | 0/0 | 3257 | 16 | 0 | 6 | 5 | 3 | 2 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0002c0002t0003 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| a0002c0002t0004 | 0/0 | 3257 | 3 | 0 | 0 | 3 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | copy fasta | chr3 | 49024707 | 49099071 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0004t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0038 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0049 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0221 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0059 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0139 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0225 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0226 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19080 | hp1 | a0002 | c0002 | t0004 | g0224 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ASW | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0002 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0090 | REF | REF | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49030471
|
T | C | 1 | a0002 | 20 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
missense_variant | MODERATE | c.2312A>G | p.Asn771Ser | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 2493/3257 | 2312/2331 | 771/776 | chr3 | 49030471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49057471
|
T | C | 1 | a0001c0004 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.729A>G | p.Gln243Gln | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/10 | 910/3257 | 729/2331 | 243/776 | chr3 | 49057471 | ||
| chr3:49057714
|
C | T | 1 | a0001c0003 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.486G>A | p.Ser162Ser | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/10 | 667/3257 | 486/2331 | 162/776 | chr3 | 49057714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49029862
|
C | CA | 2 | a0001c0001t0002a0001c0004t0002 | 5 | HG01981.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*589dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 589 | chr3 | 49029862 | |||||
| chr3:49029969
|
C | A | 1 | a0001c0001t0006 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 483 | chr3 | 49029969 | |||||
| chr3:49030186
|
C | G | 1 | a0001c0001t0005 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 266 | chr3 | 49030186 | |||||
| chr3:49030332
|
G | A | 1 | a0001c0001t0007 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 120 | chr3 | 49030332 | |||||
| chr3:49093925
|
T | TGCC | 2 | a0001c0001t0003a0002c0002t0003 | 3 | HG02071.hp1 HG02723.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-38_-36dupGGC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16909 | chr3 | 49093925 | |||||
| chr3:49093941
|
G | A | 1 | a0001c0001t0008 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16924 | chr3 | 49093941 | |||||
| chr3:49094007
|
G | C | 1 | a0002c0002t0004 | 3 | NA18954.hp1 NA19057.hp2 NA19080.hp1 |
5_prime_UTR_variant | MODIFIER | c.-117C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16990 | chr3 | 49094007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49030794
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2139-150T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030794 | ||||||
| chr3:49030898
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2139-254G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030898 | ||||||
| chr3:49030991
|
C | CT | 9 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0109others(6): Show | 9 | HG00280.hp1 HG01074.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2139-348dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030991 | ||||||
| chr3:49031351
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2139-707G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031351 | ||||||
| chr3:49031503
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0127 | 2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.2138+680A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031503 | ||||||
| chr3:49031677
|
A | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2138+506T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031677 | ||||||
| chr3:49032529
|
C | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047+93G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 8/9 | chr3 | 49032529 | ||||||
| chr3:49032960
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1895+160A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 7/9 | chr3 | 49032960 | ||||||
| chr3:49033066
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1895+54G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 7/9 | chr3 | 49033066 | ||||||
| chr3:49033339
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-111C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033339 | ||||||
| chr3:49033405
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1787-177G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033405 | ||||||
| chr3:49033420
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1787-192C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033420 | ||||||
| chr3:49033816
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0185 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1787-588C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033816 | ||||||
| chr3:49033855
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1787-627G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033855 | ||||||
| chr3:49033936
|
G | A | 2 | a0001c0001t0002g0003a0001c0004t0002g0002 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-708C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033936 | ||||||
| chr3:49033963
|
GGCAACAG others(1): Show |
G | 17 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1787-743_1787-736d others(10): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033963 | ||||||
| chr3:49033974
|
G | C | 17 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(14): Show | 17 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1787-746C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033974 | ||||||
| chr3:49034017
|
A | C | 11 | a0001c0001t0001g0080a0002c0002t0001g0038a0002c0002t0001g0040others(8): Show | 11 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1787-789T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034017 | ||||||
| chr3:49034079
|
T | TATTATTA others(6): Show |
1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1787-852_1787-851i others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTA | 127 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 127 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1787-854_1787-852d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTATTA | 16 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0093others(13): Show | 16 | HG01071.hp2 HG02109.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1787-857_1787-852d others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTATTAT others(2): Show |
10 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0072others(7): Show | 10 | HG00735.hp1 HG02145.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1787-860_1787-852d others(11): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTATTAT others(5): Show |
4 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0097others(1): Show | 4 | HG01981.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-863_1787-852d others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTATTAT others(8): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-866_1787-852d others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTATTAT others(11): Show |
1 | a0001c0001t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1787-869_1787-852d others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034079
|
T | TTTTTTA | 7 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1787-852_1787-851i others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | ||||||
| chr3:49034220
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1787-992T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034220 | ||||||
| chr3:49034391
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1787-1163C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034391 | ||||||
| chr3:49034527
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1787-1299G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034527 | ||||||
| chr3:49034645
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1787-1417G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034645 | ||||||
| chr3:49034660
|
GT | G | 8 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1787-1433delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034660 | ||||||
| chr3:49034752
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1787-1524G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034752 | ||||||
| chr3:49034795
|
T | C | 10 | a0002c0002t0001g0038a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1787-1567A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034795 | ||||||
| chr3:49034802
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-1574T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034802 | ||||||
| chr3:49035154
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1787-1926G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035154 | ||||||
| chr3:49035197
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0162a0001c0001t0001g0210 | 3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1787-1969T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035197 | ||||||
| chr3:49035911
|
C | CA | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(25): Show | 28 | HG00544.hp2 HG00609.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.1787-2684dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035911 | ||||||
| chr3:49035911
|
C | CAA | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1787-2685_1787-268 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035911 | ||||||
| chr3:49035922
|
A | AC | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1787-2695_1787-269 others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035922 | ||||||
| chr3:49035922
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1787-2694T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035922 | ||||||
| chr3:49035942
|
G | C | 1 | a0002c0002t0001g0044 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1787-2714C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035942 | ||||||
| chr3:49036189
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1787-2961T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036189 | ||||||
| chr3:49036238
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1787-3010A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036238 | ||||||
| chr3:49036696
|
C | CA | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3469dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036696 | ||||||
| chr3:49036696
|
CA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.1787-3469delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036696 | ||||||
| chr3:49036714
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3486C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036714 | ||||||
| chr3:49037073
|
T | TA | 129 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0032others(126): Show | 129 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1787-3846dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | ||||||
| chr3:49037073
|
T | TAA | 6 | a0001c0001t0001g0143a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1787-3847_1787-384 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | ||||||
| chr3:49037073
|
T | TAAA | 16 | a0002c0002t0001g0010a0002c0002t0001g0038a0002c0002t0001g0039others(13): Show | 16 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1787-3848_1787-384 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | ||||||
| chr3:49037073
|
TA | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0054others(2): Show | 5 | HG02735.hp2 HG02809.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3846delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | ||||||
| chr3:49037850
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1787-4622C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037850 | ||||||
| chr3:49037939
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-4711C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037939 | ||||||
| chr3:49038001
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1787-4773T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038001 | ||||||
| chr3:49038080
|
A | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1787-4852T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038080 | ||||||
| chr3:49038170
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-4942G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038170 | ||||||
| chr3:49038310
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1787-5082A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038310 | ||||||
| chr3:49038555
|
C | G | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1787-5327G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038555 | ||||||
| chr3:49038638
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.1787-5410A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038638 | ||||||
| chr3:49038659
|
G | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1787-5431C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038659 | ||||||
| chr3:49038764
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1787-5536G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038764 | ||||||
| chr3:49039249
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+5141T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039249 | ||||||
| chr3:49039318
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+5072A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039318 | ||||||
| chr3:49039336
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1786+5054C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039336 | ||||||
| chr3:49039446
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1786+4944G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039446 | ||||||
| chr3:49039451
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1786+4939G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039451 | ||||||
| chr3:49039463
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1786+4927A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039463 | ||||||
| chr3:49039515
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1786+4875G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039515 | ||||||
| chr3:49039517
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+4873G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039517 | ||||||
| chr3:49039618
|
C | CA | 9 | a0001c0001t0001g0111a0001c0001t0001g0153a0001c0001t0001g0191others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1786+4771dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039618 | ||||||
| chr3:49039618
|
CA | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0079others(3): Show | 6 | HG00733.hp1 HG01070.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+4771delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039618 | ||||||
| chr3:49039727
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1786+4663T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039727 | ||||||
| chr3:49039762
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0025others(1): Show | 4 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786+4628C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039762 | ||||||
| chr3:49039922
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1786+4468G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039922 | ||||||
| chr3:49039987
|
A | C | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0126others(2): Show | 5 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+4403T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039987 | ||||||
| chr3:49040001
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1786+4389T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040001 | ||||||
| chr3:49040333
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1786+4057G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040333 | ||||||
| chr3:49040605
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1786+3785A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040605 | ||||||
| chr3:49040648
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1786+3742G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040648 | ||||||
| chr3:49040961
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+3429G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040961 | ||||||
| chr3:49041050
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786+3340G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041050 | ||||||
| chr3:49041163
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0148 | 2 | NA19012.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1786+3227A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041163 | ||||||
| chr3:49041339
|
ATG | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1786+3049_1786+305 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041339 | ||||||
| chr3:49041491
|
C | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+2899G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041491 | ||||||
| chr3:49041618
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+2772C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041618 | ||||||
| chr3:49041643
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1786+2747A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041643 | ||||||
| chr3:49041670
|
ACTCAGGC others(460): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1786+2253_1786+271 others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041670 | ||||||
| chr3:49041672
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1786+2718A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041672 | ||||||
| chr3:49041974
|
T | C | 1 | a0002c0002t0001g0044 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1786+2416A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041974 | ||||||
| chr3:49042053
|
G | A | 27 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0076others(24): Show | 27 | HG00544.hp1 HG00735.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1786+2337C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042053 | ||||||
| chr3:49042062
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1786+2328G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042062 | ||||||
| chr3:49042076
|
G | GT | 22 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0032others(19): Show | 22 | HG01099.hp1 HG01099.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1786+2313dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042076 | ||||||
| chr3:49042095
|
C | CG | 38 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0025others(35): Show | 38 | HG01099.hp1 HG01099.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1786+2294dupC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042095 | ||||||
| chr3:49042168
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+2222C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042168 | ||||||
| chr3:49042444
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+1946G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042444 | ||||||
| chr3:49042466
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1786+1924G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042466 | ||||||
| chr3:49042580
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+1810C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042580 | ||||||
| chr3:49042745
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1786+1645C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042745 | ||||||
| chr3:49042785
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1786+1605G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042785 | ||||||
| chr3:49043063
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0096others(1): Show | 4 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1327T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043063 | ||||||
| chr3:49043465
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1786+925G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043465 | ||||||
| chr3:49043496
|
C | CA | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1786+893dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | ||||||
| chr3:49043496
|
C | CAA | 13 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0083others(10): Show | 13 | HG01261.hp1 HG01981.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1786+892_1786+893d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | ||||||
| chr3:49043496
|
CA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0033others(2): Show | 5 | HG01515.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+893delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | ||||||
| chr3:49043496
|
CAAAAAAA others(3): Show |
C | 61 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0076others(58): Show | 61 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1786+884_1786+893d others(12): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | ||||||
| chr3:49043496
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0174 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1786+883_1786+893d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | ||||||
| chr3:49043554
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1786+836C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043554 | ||||||
| chr3:49043814
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1786+576A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043814 | ||||||
| chr3:49044053
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1786+337C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49044053 | ||||||
| chr3:49044609
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1672-105A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044609 | ||||||
| chr3:49044703
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1672-199C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044703 | ||||||
| chr3:49044810
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1672-306T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044810 | ||||||
| chr3:49044852
|
C | CA | 7 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0079others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-349dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044852 | ||||||
| chr3:49045011
|
A | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0079others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-507T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045011 | ||||||
| chr3:49045326
|
C | CA | 43 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0016others(40): Show | 43 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1672-823dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | ||||||
| chr3:49045326
|
C | CAA | 22 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0057others(19): Show | 22 | HG01074.hp2 HG01243.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.1672-824_1672-823d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | ||||||
| chr3:49045326
|
CAAAA | C | 16 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(13): Show | 16 | HG01243.hp1 HG01952.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1672-826_1672-823d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | ||||||
| chr3:49045326
|
CAAAAA | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1672-827_1672-823d others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | ||||||
| chr3:49045512
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1671+913G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045512 | ||||||
| chr3:49045688
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1671+737G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045688 | ||||||
| chr3:49045831
|
G | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0176 | 2 | HG02083.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1671+594C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045831 | ||||||
| chr3:49045916
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1671+509G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045916 | ||||||
| chr3:49045991
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0160 | 2 | HG02015.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1671+434A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045991 | ||||||
| chr3:49046133
|
G | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG00140.hp2 HG00280.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+292C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046133 | ||||||
| chr3:49046262
|
T | TA | 47 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0071others(44): Show | 47 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1671+162dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046262 | ||||||
| chr3:49046288
|
T | C | 10 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 10 | HG00609.hp1 HG02015.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1671+137A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046288 | ||||||
| chr3:49046833
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516+236T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 4/9 | chr3 | 49046833 | ||||||
| chr3:49046846
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1516+223C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 4/9 | chr3 | 49046846 | ||||||
| chr3:49047345
|
G | GA | 6 | a0001c0001t0001g0056a0001c0001t0001g0100a0001c0001t0001g0122others(3): Show | 6 | HG02071.hp2 NA18944.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-100dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047345 | ||||||
| chr3:49047397
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1339-151A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047397 | ||||||
| chr3:49047424
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1339-178G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047424 | ||||||
| chr3:49047479
|
G | GT | 27 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0034others(24): Show | 27 | HG00140.hp2 HG01928.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.1339-234dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047479 | ||||||
| chr3:49047479
|
GT | G | 6 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG02735.hp2 HG03453.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-234delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047479 | ||||||
| chr3:49047541
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1339-295A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047541 | ||||||
| chr3:49047570
|
G | A | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1339-324C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047570 | ||||||
| chr3:49047640
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1339-394G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047640 | ||||||
| chr3:49047679
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1339-433G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047679 | ||||||
| chr3:49047779
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1339-533C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047779 | ||||||
| chr3:49047893
|
C | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-647G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047893 | ||||||
| chr3:49048040
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1339-794G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048040 | ||||||
| chr3:49048063
|
TG | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-818delC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048063 | ||||||
| chr3:49048118
|
ATTTC | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-876_1339-873d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048118 | ||||||
| chr3:49048130
|
CT | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1339-885delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048130 | ||||||
| chr3:49048196
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1339-950C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048196 | ||||||
| chr3:49048289
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1339-1043G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048289 | ||||||
| chr3:49048382
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1339-1136G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048382 | ||||||
| chr3:49048477
|
T | TA | 8 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0191others(5): Show | 8 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-1232dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048477 | ||||||
| chr3:49048490
|
A | C | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1339-1244T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048490 | ||||||
| chr3:49048498
|
A | C | 30 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(27): Show | 30 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1339-1252T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048498 | ||||||
| chr3:49048780
|
T | TC | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1339-1535dupG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048780 | ||||||
| chr3:49048782
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1339-1536A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048782 | ||||||
| chr3:49048801
|
C | CA | 7 | a0001c0001t0001g0089a0001c0001t0001g0112a0001c0001t0001g0160others(4): Show | 7 | HG02015.hp1 HG02818.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-1556dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048801 | ||||||
| chr3:49048826
|
C | T | 21 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1339-1580G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048826 | ||||||
| chr3:49048954
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1339-1708A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048954 | ||||||
| chr3:49049004
|
C | G | 1 | a0001c0003t0001g0095 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1339-1758G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049004 | ||||||
| chr3:49049140
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1339-1894G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049140 | ||||||
| chr3:49049297
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1339-2051A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049297 | ||||||
| chr3:49049377
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1339-2131C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049377 | ||||||
| chr3:49049694
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2448G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049694 | ||||||
| chr3:49049696
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2450G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049696 | ||||||
| chr3:49049697
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2451G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049697 | ||||||
| chr3:49049698
|
A | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2452T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049698 | ||||||
| chr3:49049700
|
G | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2454C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049700 | ||||||
| chr3:49049703
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2457C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049703 | ||||||
| chr3:49049704
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2458C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049704 | ||||||
| chr3:49049705
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2459G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049705 | ||||||
| chr3:49049706
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2460G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049706 | ||||||
| chr3:49049708
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2462C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049708 | ||||||
| chr3:49049709
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2463C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049709 | ||||||
| chr3:49049713
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2467C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049713 | ||||||
| chr3:49049715
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2469G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049715 | ||||||
| chr3:49049716
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2470A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049716 | ||||||
| chr3:49049718
|
A | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2472T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049718 | ||||||
| chr3:49049725
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2479G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049725 | ||||||
| chr3:49049726
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2480C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049726 | ||||||
| chr3:49049727
|
A | G | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2481T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049727 | ||||||
| chr3:49049729
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2483G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049729 | ||||||
| chr3:49049730
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2484A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049730 | ||||||
| chr3:49049733
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2487C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049733 | ||||||
| chr3:49049734
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2488C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049734 | ||||||
| chr3:49049735
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2489A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049735 | ||||||
| chr3:49049738
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2492A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049738 | ||||||
| chr3:49049739
|
C | G | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2493G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049739 | ||||||
| chr3:49049741
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0169 | 3 | HG01099.hp2 HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1339-2495C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049741 | ||||||
| chr3:49049741
|
G | C | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2495C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049741 | ||||||
| chr3:49049742
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2496A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049742 | ||||||
| chr3:49049744
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2498A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049744 | ||||||
| chr3:49049745
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2499C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049745 | ||||||
| chr3:49049746
|
C | G | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2500G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049746 | ||||||
| chr3:49049747
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2501G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049747 | ||||||
| chr3:49049748
|
T | C | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2502A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049748 | ||||||
| chr3:49049750
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2504C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049750 | ||||||
| chr3:49049751
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2505C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049751 | ||||||
| chr3:49049752
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2506G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049752 | ||||||
| chr3:49049753
|
C | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2507G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049753 | ||||||
| chr3:49049756
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2510G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049756 | ||||||
| chr3:49049757
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2511G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049757 | ||||||
| chr3:49049771
|
T | G | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2525A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049771 | ||||||
| chr3:49049772
|
A | G | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2526T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049772 | ||||||
| chr3:49049778
|
G | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-2532C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049778 | ||||||
| chr3:49049779
|
T | A | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2533A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049779 | ||||||
| chr3:49049793
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1339-2547G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049793 | ||||||
| chr3:49049805
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1339-2559C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049805 | ||||||
| chr3:49050248
|
C | CA | 10 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0052others(7): Show | 10 | HG00544.hp2 HG01261.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1339-3003dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAA | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1339-3004_1339-300 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1339-3012_1339-300 others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0214a0001c0001t0001g0218 | 3 | HG01516.hp1 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1339-3013_1339-300 others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1339-3014_1339-300 others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0151 | 3 | HG02809.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1339-3015_1339-300 others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1339-3016_1339-300 others(18): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0106a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02109.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-3017_1339-300 others(19): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1339-3018_1339-300 others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1339-3020_1339-300 others(22): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0217 | 2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1339-3023_1339-300 others(25): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0213 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1339-3024_1339-300 others(26): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0142 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1339-3026_1339-300 others(28): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0091 | 2 | HG01261.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1339-3027_1339-300 others(29): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(31): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(33): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(36): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(37): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1339-3003_1339-300 others(40): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(41): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
CAAA | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0173a0001c0001t0001g0175others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-3005_1339-300 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
CAAAA | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0056others(90): Show | 93 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1339-3006_1339-300 others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050248
|
CAAAAA | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(4): Show | 7 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-3007_1339-300 others(9): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | ||||||
| chr3:49050422
|
C | CA | 34 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0037others(31): Show | 34 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1339-3177dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | ||||||
| chr3:49050422
|
C | CAA | 8 | a0001c0001t0001g0202a0001c0001t0002g0003a0001c0001t0002g0219others(5): Show | 8 | HG01070.hp1 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-3178_1339-317 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | ||||||
| chr3:49050422
|
CA | C | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1339-3177delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | ||||||
| chr3:49050422
|
CAA | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0126others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-3178_1339-317 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | ||||||
| chr3:49050422
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0169 | 3 | HG01099.hp2 HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1339-3189_1339-317 others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | ||||||
| chr3:49050503
|
C | T | 1 | a0001c0004t0002g0002 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1339-3257G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050503 | ||||||
| chr3:49050527
|
C | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1339-3281G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050527 | ||||||
| chr3:49050579
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-3333C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050579 | ||||||
| chr3:49050592
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1339-3346T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050592 | ||||||
| chr3:49050679
|
T | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1339-3433A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050679 | ||||||
| chr3:49050694
|
AAAC | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 200 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.1339-3451_1339-344 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050694 | ||||||
| chr3:49050923
|
T | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-3677A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050923 | ||||||
| chr3:49050926
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1339-3680T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050926 | ||||||
| chr3:49050986
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-3740A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050986 | ||||||
| chr3:49051161
|
C | T | 1 | a0001c0001t0006g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1339-3915G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051161 | ||||||
| chr3:49051238
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1339-3992G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051238 | ||||||
| chr3:49051324
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1339-4078A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051324 | ||||||
| chr3:49051344
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1339-4098C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051344 | ||||||
| chr3:49051584
|
G | GC | 43 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1339-4339dupG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | ||||||
| chr3:49051584
|
G | GCC | 41 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0050others(38): Show | 41 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1339-4340_1339-433 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | ||||||
| chr3:49051584
|
GC | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 37 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1339-4339delG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | ||||||
| chr3:49051587
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1339-4341G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051587 | ||||||
| chr3:49051594
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1339-4348G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051594 | ||||||
| chr3:49051631
|
C | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(3): Show | 6 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-4385G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051631 | ||||||
| chr3:49051634
|
A | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1339-4388T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051634 | ||||||
| chr3:49051694
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1339-4448C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051694 | ||||||
| chr3:49051935
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1339-4689C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051935 | ||||||
| chr3:49052004
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1339-4758T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052004 | ||||||
| chr3:49052023
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1339-4777C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052023 | ||||||
| chr3:49052294
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1338+4568G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052294 | ||||||
| chr3:49052340
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1338+4522C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052340 | ||||||
| chr3:49052911
|
T | C | 2 | a0001c0001t0001g0140a0001c0003t0001g0095 | 2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1338+3951A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052911 | ||||||
| chr3:49053070
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+3792G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053070 | ||||||
| chr3:49053187
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+3675C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053187 | ||||||
| chr3:49053263
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.1338+3599A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053263 | ||||||
| chr3:49053486
|
C | CA | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1338+3375dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | ||||||
| chr3:49053486
|
C | CAA | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 55 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1338+3374_1338+337 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | ||||||
| chr3:49053486
|
C | CAAA | 5 | a0001c0001t0001g0035a0001c0001t0001g0140a0001c0001t0001g0168others(2): Show | 5 | HG01515.hp1 HG01517.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+3373_1338+337 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | ||||||
| chr3:49053506
|
C | A | 1 | a0002c0002t0003g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1338+3356G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053506 | ||||||
| chr3:49053507
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1338+3355T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053507 | ||||||
| chr3:49053990
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1338+2872C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053990 | ||||||
| chr3:49054270
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0134others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+2592A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054270 | ||||||
| chr3:49054339
|
G | A | 22 | a0001c0001t0001g0035a0001c0001t0001g0188a0001c0001t0001g0189others(19): Show | 22 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1338+2523C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054339 | ||||||
| chr3:49054659
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1338+2203A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054659 | ||||||
| chr3:49055005
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1338+1857T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055005 | ||||||
| chr3:49055241
|
T | G | 1 | a0001c0001t0002g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1338+1621A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055241 | ||||||
| chr3:49055515
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1338+1347A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055515 | ||||||
| chr3:49055586
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+1276G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055586 | ||||||
| chr3:49055648
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG00544.hp2 HG02735.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+1214G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055648 | ||||||
| chr3:49055944
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1338+918T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055944 | ||||||
| chr3:49056124
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1338+738A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056124 | ||||||
| chr3:49056177
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0181 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1338+685A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056177 | ||||||
| chr3:49056234
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1338+628T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056234 | ||||||
| chr3:49056272
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1338+590G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056272 | ||||||
| chr3:49056279
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+583G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056279 | ||||||
| chr3:49056504
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1338+358A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056504 | ||||||
| chr3:49056505
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1338+357T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056505 | ||||||
| chr3:49056505
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1338+357T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056505 | ||||||
| chr3:49058158
|
T | A | 1 | a0002c0002t0001g0010 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.310-268A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058158 | ||||||
| chr3:49058256
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.310-366A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058256 | ||||||
| chr3:49058613
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-723C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058613 | ||||||
| chr3:49058662
|
CTT | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-774_310-773del others(2): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058662 | ||||||
| chr3:49058961
|
CT | C | 35 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0050others(32): Show | 35 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.310-1072delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058961 | ||||||
| chr3:49059002
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.310-1112G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059002 | ||||||
| chr3:49059055
|
G | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0150others(2): Show | 5 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-1165C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059055 | ||||||
| chr3:49059105
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.310-1215C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059105 | ||||||
| chr3:49059415
|
C | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.310-1525G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059415 | ||||||
| chr3:49059564
|
C | T | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.310-1674G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059564 | ||||||
| chr3:49059606
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-1716C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059606 | ||||||
| chr3:49059626
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-1736C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059626 | ||||||
| chr3:49059715
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.310-1825G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059715 | ||||||
| chr3:49059794
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0005g0139 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.310-1904G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059794 | ||||||
| chr3:49059901
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0142 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.310-2011A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059901 | ||||||
| chr3:49059988
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-2098C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059988 | ||||||
| chr3:49060041
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-2151G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060041 | ||||||
| chr3:49060149
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-2259G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060149 | ||||||
| chr3:49060267
|
C | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088 | 3 | HG01070.hp2 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.310-2377G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060267 | ||||||
| chr3:49060322
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-2432A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060322 | ||||||
| chr3:49060328
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.310-2438C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060328 | ||||||
| chr3:49060350
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.310-2460G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060350 | ||||||
| chr3:49060519
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0162a0001c0001t0001g0210 | 3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.310-2629C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060519 | ||||||
| chr3:49060695
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-2805G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060695 | ||||||
| chr3:49060980
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310-3090A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060980 | ||||||
| chr3:49061134
|
T | TA | 16 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0031others(13): Show | 16 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-3245dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
T | TAAA | 6 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0003g0221others(3): Show | 6 | HG02071.hp1 NA18747.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-3247_310-3245d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TA | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0018others(20): Show | 23 | HG00609.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.310-3245delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TAA | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG02071.hp2 HG02280.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.310-3246_310-3245d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TAAA | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0071others(23): Show | 26 | HG00140.hp2 HG01074.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.310-3247_310-3245d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TAAAA | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.310-3248_310-3245d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TAAAAA | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0061others(4): Show | 7 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-3249_310-3245d others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061134
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.310-3258_310-3245d others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | ||||||
| chr3:49061308
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310-3418G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061308 | ||||||
| chr3:49061743
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-3853A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061743 | ||||||
| chr3:49062002
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-4112C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062002 | ||||||
| chr3:49062163
|
T | C | 14 | a0001c0001t0001g0071a0001c0001t0001g0086a0001c0001t0001g0087others(11): Show | 14 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.310-4273A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062163 | ||||||
| chr3:49062282
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-4392C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062282 | ||||||
| chr3:49062372
|
C | CT | 12 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(9): Show | 12 | HG00735.hp1 HG01346.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.310-4483dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062372 | ||||||
| chr3:49062516
|
A | G | 2 | a0002c0002t0001g0043a0002c0002t0001g0065 | 2 | NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.310-4626T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062516 | ||||||
| chr3:49062729
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.310-4839G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062729 | ||||||
| chr3:49062730
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-4840C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062730 | ||||||
| chr3:49062776
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.310-4886C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062776 | ||||||
| chr3:49062831
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.310-4941G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062831 | ||||||
| chr3:49062831
|
C | T | 2 | a0001c0001t0002g0003a0001c0004t0002g0002 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-4941G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062831 | ||||||
| chr3:49062842
|
T | C | 1 | a0002c0002t0001g0044 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.310-4952A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062842 | ||||||
| chr3:49062872
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.310-4982A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062872 | ||||||
| chr3:49062957
|
G | A | 1 | a0001c0004t0002g0002 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.310-5067C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062957 | ||||||
| chr3:49063128
|
G | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-5238C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49063128 | ||||||
| chr3:49064183
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.310-6293C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064183 | ||||||
| chr3:49064234
|
A | AT | 21 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0062others(18): Show | 21 | HG00735.hp2 HG01261.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.310-6345dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | ||||||
| chr3:49064234
|
AT | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0108others(8): Show | 11 | HG01256.hp1 HG01256.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-6345delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | ||||||
| chr3:49064234
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-6355_310-6345d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | ||||||
| chr3:49064356
|
C | T | 1 | a0001c0001t0008g0223 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.310-6466G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064356 | ||||||
| chr3:49064568
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.310-6678T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064568 | ||||||
| chr3:49064681
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.310-6791G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064681 | ||||||
| chr3:49064756
|
G | A | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.310-6866C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064756 | ||||||
| chr3:49064801
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-6911T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064801 | ||||||
| chr3:49064843
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-6953G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064843 | ||||||
| chr3:49065103
|
A | G | 1 | a0001c0001t0006g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.310-7213T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065103 | ||||||
| chr3:49065346
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.310-7456A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065346 | ||||||
| chr3:49065538
|
TCA | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18963.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.310-7650_310-7649d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065538 | ||||||
| chr3:49065568
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.310-7678T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065568 | ||||||
| chr3:49065809
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-7919A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065809 | ||||||
| chr3:49066244
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.310-8354A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066244 | ||||||
| chr3:49066281
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8391G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066281 | ||||||
| chr3:49066434
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.310-8544A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066434 | ||||||
| chr3:49066443
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310-8553A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066443 | ||||||
| chr3:49066460
|
CT | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8571delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066460 | ||||||
| chr3:49066466
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8576A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066466 | ||||||
| chr3:49066476
|
T | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0175 | 2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.310-8586A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066476 | ||||||
| chr3:49066558
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.310-8668C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066558 | ||||||
| chr3:49066583
|
GCCT | G | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-8696_310-8694d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066583 | ||||||
| chr3:49066701
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0173 | 2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.310-8811G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066701 | ||||||
| chr3:49066843
|
G | C | 5 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-8953C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066843 | ||||||
| chr3:49066864
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-8974G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066864 | ||||||
| chr3:49066964
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.310-9074C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066964 | ||||||
| chr3:49066969
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0070 | 3 | NA19003.hp1 NA19012.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.310-9079G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066969 | ||||||
| chr3:49067149
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-9259G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067149 | ||||||
| chr3:49067395
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.309+9314C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067395 | ||||||
| chr3:49067703
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.309+9006T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067703 | ||||||
| chr3:49067964
|
T | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0188others(20): Show | 23 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.309+8745A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067964 | ||||||
| chr3:49068108
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.309+8601A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068108 | ||||||
| chr3:49068294
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.309+8415G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068294 | ||||||
| chr3:49068357
|
T | A | 1 | a0002c0002t0001g0010 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.309+8352A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068357 | ||||||
| chr3:49068432
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.309+8277A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068432 | ||||||
| chr3:49068450
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.309+8259A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068450 | ||||||
| chr3:49068453
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+8256C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068453 | ||||||
| chr3:49068454
|
T | A | 4 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0219others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+8255A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068454 | ||||||
| chr3:49068466
|
T | TA | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 182 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.309+8242dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068466 | ||||||
| chr3:49068466
|
T | TAA | 6 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0032others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+8241_309+8242d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068466 | ||||||
| chr3:49068634
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0002g0219 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.309+8075G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068634 | ||||||
| chr3:49068753
|
T | C | 28 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0076others(25): Show | 28 | HG00544.hp1 HG00735.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.309+7956A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068753 | ||||||
| chr3:49068908
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+7801C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068908 | ||||||
| chr3:49068942
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.309+7767T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068942 | ||||||
| chr3:49069098
|
A | T | 2 | a0002c0002t0004g0224a0002c0002t0004g0226 | 2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.309+7611T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069098 | ||||||
| chr3:49069101
|
A | AT | 10 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0067others(7): Show | 10 | HG01099.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+7607dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069101 | ||||||
| chr3:49069101
|
A | T | 20 | a0001c0001t0001g0052a0002c0002t0001g0038a0002c0002t0001g0039others(17): Show | 20 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.309+7608T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069101 | ||||||
| chr3:49069103
|
TA | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0111a0001c0001t0001g0137others(3): Show | 6 | HG03017.hp1 HG03471.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+7605delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069103 | ||||||
| chr3:49069104
|
A | AT | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 22 | HG00609.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+7604dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069104 | ||||||
| chr3:49069104
|
A | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0037others(31): Show | 34 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.309+7605T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069104 | ||||||
| chr3:49069107
|
A | AT | 33 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(30): Show | 33 | HG00140.hp2 HG01192.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.309+7601dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | ||||||
| chr3:49069107
|
A | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.309+7602T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | ||||||
| chr3:49069107
|
AT | A | 21 | a0001c0001t0001g0035a0001c0001t0001g0188a0001c0001t0001g0189others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+7601delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | ||||||
| chr3:49069109
|
T | TA | 66 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0071others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.309+7599_309+7600i others(3): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069109 | ||||||
| chr3:49069110
|
T | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0110others(1): Show | 4 | HG01168.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+7599A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069110 | ||||||
| chr3:49069111
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.309+7598A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069111 | ||||||
| chr3:49069112
|
T | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0109others(4): Show | 7 | HG02083.hp1 HG03942.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+7597A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069112 | ||||||
| chr3:49069113
|
T | A | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+7596A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069113 | ||||||
| chr3:49069124
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.309+7585C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069124 | ||||||
| chr3:49069292
|
C | T | 4 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0219others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+7417G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069292 | ||||||
| chr3:49069296
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.309+7413C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069296 | ||||||
| chr3:49069543
|
A | AT | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.309+7165dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069543 | ||||||
| chr3:49069543
|
A | ATT | 12 | a0001c0001t0001g0070a0001c0001t0001g0091a0001c0001t0001g0092others(9): Show | 12 | HG01496.hp1 HG01981.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+7164_309+7165d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069543 | ||||||
| chr3:49069543
|
A | T | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.309+7166T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069543 | ||||||
| chr3:49070038
|
A | AT | 7 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0132others(4): Show | 7 | HG00735.hp1 HG01261.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+6670dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070038 | ||||||
| chr3:49070101
|
G | A | 2 | a0001c0001t0001g0140a0001c0003t0001g0095 | 2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.309+6608C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070101 | ||||||
| chr3:49070133
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.309+6576C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070133 | ||||||
| chr3:49070145
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.309+6564G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070145 | ||||||
| chr3:49070226
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.309+6483A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070226 | ||||||
| chr3:49070280
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.309+6429G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070280 | ||||||
| chr3:49070335
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0173 | 2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.309+6374C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070335 | ||||||
| chr3:49070418
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+6291G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070418 | ||||||
| chr3:49070861
|
A | G | 4 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0219others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+5848T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070861 | ||||||
| chr3:49070995
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 180 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.309+5714A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070995 | ||||||
| chr3:49071068
|
CT | C | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.309+5640delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071068 | ||||||
| chr3:49071104
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.309+5605C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071104 | ||||||
| chr3:49071166
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+5543C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071166 | ||||||
| chr3:49071228
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.309+5481G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071228 | ||||||
| chr3:49071452
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.309+5257T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071452 | ||||||
| chr3:49071634
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.309+5075C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071634 | ||||||
| chr3:49071846
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.309+4863G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071846 | ||||||
| chr3:49072086
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.309+4623A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072086 | ||||||
| chr3:49072152
|
G | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+4557C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072152 | ||||||
| chr3:49072160
|
A | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.309+4549T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072160 | ||||||
| chr3:49072191
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.309+4518G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072191 | ||||||
| chr3:49072192
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0096others(1): Show | 4 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+4517C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072192 | ||||||
| chr3:49072486
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 180 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.309+4223C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072486 | ||||||
| chr3:49073278
|
C | T | 1 | a0002c0002t0001g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.309+3431G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073278 | ||||||
| chr3:49073456
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.309+3253A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073456 | ||||||
| chr3:49073625
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.309+3084A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073625 | ||||||
| chr3:49073626
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.309+3083T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073626 | ||||||
| chr3:49073760
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.309+2949A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073760 | ||||||
| chr3:49073834
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0162a0001c0001t0001g0210 | 3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.309+2875T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073834 | ||||||
| chr3:49074077
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+2632A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074077 | ||||||
| chr3:49074126
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.309+2583G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074126 | ||||||
| chr3:49074320
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.309+2389G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074320 | ||||||
| chr3:49074429
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0159 | 3 | HG01168.hp2 HG01256.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.309+2280T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074429 | ||||||
| chr3:49074639
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.309+2070G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074639 | ||||||
| chr3:49074745
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1964C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074745 | ||||||
| chr3:49074913
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309+1796T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074913 | ||||||
| chr3:49074999
|
C | T | 4 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0219others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+1710G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074999 | ||||||
| chr3:49075025
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0145 | 2 | HG00609.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.309+1684G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075025 | ||||||
| chr3:49075154
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.309+1555A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075154 | ||||||
| chr3:49075295
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.309+1414G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075295 | ||||||
| chr3:49075330
|
C | CA | 9 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0124others(6): Show | 9 | HG00544.hp2 HG02071.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+1378dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075330 | ||||||
| chr3:49075330
|
CA | C | 7 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0177others(4): Show | 7 | HG01256.hp1 HG02965.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+1378delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075330 | ||||||
| chr3:49075401
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.309+1308T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075401 | ||||||
| chr3:49075488
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309+1221C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075488 | ||||||
| chr3:49075568
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0005g0139 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.309+1141A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075568 | ||||||
| chr3:49075651
|
A | AAAC | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+1057_309+1058i others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075651 | ||||||
| chr3:49075966
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.309+743C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075966 | ||||||
| chr3:49076235
|
T | C | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+474A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076235 | ||||||
| chr3:49076280
|
C | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+429G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076280 | ||||||
| chr3:49076296
|
C | T | 10 | a0002c0002t0001g0038a0002c0002t0001g0040a0002c0002t0001g0041others(7): Show | 10 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+413G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076296 | ||||||
| chr3:49076322
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+387C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076322 | ||||||
| chr3:49076404
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.309+305C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076404 | ||||||
| chr3:49076488
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+221A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076488 | ||||||
| chr3:49076524
|
TA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.309+184delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076524 | ||||||
| chr3:49076632
|
TGATG | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+73_309+76delCA others(2): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076632 | ||||||
| chr3:49077111
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-21-73G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077111 | ||||||
| chr3:49077680
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-642A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077680 | ||||||
| chr3:49077957
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-21-919G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077957 | ||||||
| chr3:49078095
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21-1057T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078095 | ||||||
| chr3:49078386
|
C | CT | 113 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.-21-1349dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | ||||||
| chr3:49078386
|
C | CTT | 27 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0070others(24): Show | 27 | HG00609.hp1 HG00735.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.-21-1350_-21-1349d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | ||||||
| chr3:49078386
|
CT | C | 12 | a0001c0001t0001g0113a0001c0001t0002g0036a0002c0002t0001g0040others(9): Show | 12 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21-1349delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | ||||||
| chr3:49078515
|
C | T | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-21-1477G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078515 | ||||||
| chr3:49078694
|
C | CT | 25 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0032others(22): Show | 25 | HG00544.hp1 HG00735.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-21-1657dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078694 | ||||||
| chr3:49078694
|
CT | C | 23 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0001t0001g0190others(20): Show | 23 | HG01074.hp2 HG01243.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21-1657delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078694 | ||||||
| chr3:49079001
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-21-1963G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079001 | ||||||
| chr3:49079134
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-21-2096G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079134 | ||||||
| chr3:49079237
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0185 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-2199T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079237 | ||||||
| chr3:49079458
|
T | C | 2 | a0002c0002t0001g0039a0002c0002t0001g0064 | 2 | HG00609.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.-21-2420A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079458 | ||||||
| chr3:49079748
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-21-2710C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079748 | ||||||
| chr3:49080028
|
C | CA | 162 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(159): Show | 162 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-21-2991dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080028 | ||||||
| chr3:49080028
|
C | CAA | 5 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0152others(2): Show | 5 | HG01981.hp1 HG03704.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-2992_-21-2991d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080028 | ||||||
| chr3:49080139
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-3101C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080139 | ||||||
| chr3:49080216
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-21-3178C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080216 | ||||||
| chr3:49080217
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-21-3179T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080217 | ||||||
| chr3:49080580
|
G | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-3542C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080580 | ||||||
| chr3:49080622
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21-3584G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080622 | ||||||
| chr3:49080854
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-21-3816A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080854 | ||||||
| chr3:49080966
|
C | CA | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 98 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-21-3929dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080966 | ||||||
| chr3:49080966
|
C | CAA | 56 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0050others(53): Show | 56 | HG00544.hp2 HG00639.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.-21-3930_-21-3929d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080966 | ||||||
| chr3:49081203
|
G | A | 21 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21-4165C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081203 | ||||||
| chr3:49081279
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-21-4241A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081279 | ||||||
| chr3:49081413
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0172 | 2 | NA18961.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-21-4375A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081413 | ||||||
| chr3:49081414
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0172 | 2 | NA18961.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-21-4376G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081414 | ||||||
| chr3:49081416
|
TA | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0082others(10): Show | 13 | HG01070.hp2 HG01496.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21-4379delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081416 | ||||||
| chr3:49081421
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-4383T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081421 | ||||||
| chr3:49081811
|
A | AT | 9 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0070others(6): Show | 9 | HG01515.hp1 HG02572.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-4774dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081811 | ||||||
| chr3:49082007
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-21-4969G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082007 | ||||||
| chr3:49082179
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21-5141G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082179 | ||||||
| chr3:49082219
|
G | A | 2 | a0001c0001t0001g0140a0001c0003t0001g0095 | 2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-21-5181C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082219 | ||||||
| chr3:49082573
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0096others(3): Show | 6 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-5535A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082573 | ||||||
| chr3:49082607
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 27 | HG00639.hp2 HG00738.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-21-5569T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082607 | ||||||
| chr3:49082694
|
G | GACC | 10 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(7): Show | 10 | HG00544.hp2 HG02280.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-5659_-21-5657d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082694 | ||||||
| chr3:49082811
|
C | T | 2 | a0001c0001t0002g0003a0001c0004t0002g0002 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-21-5773G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082811 | ||||||
| chr3:49082838
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-21-5800A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082838 | ||||||
| chr3:49082894
|
CA | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG01515.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-5857delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082894 | ||||||
| chr3:49083183
|
C | T | 1 | a0002c0002t0001g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-21-6145G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083183 | ||||||
| chr3:49083204
|
C | CA | 107 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-21-6167dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083204 | ||||||
| chr3:49083204
|
C | CAA | 7 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0093others(4): Show | 7 | HG02129.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-6168_-21-6167d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083204 | ||||||
| chr3:49083220
|
A | AAG | 18 | a0001c0001t0001g0056a0001c0001t0001g0075a0001c0001t0001g0078others(15): Show | 18 | HG01192.hp1 HG01192.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21-6183_-21-6182i others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083220 | ||||||
| chr3:49083220
|
A | G | 1 | a0002c0002t0001g0065 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-21-6182T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083220 | ||||||
| chr3:49083221
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0073a0001c0001t0001g0074others(5): Show | 8 | HG02004.hp1 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-6183C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083221 | ||||||
| chr3:49083222
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-21-6184C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083222 | ||||||
| chr3:49083301
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21-6263A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083301 | ||||||
| chr3:49083370
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-6332C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083370 | ||||||
| chr3:49083469
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-6431A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083469 | ||||||
| chr3:49083664
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-21-6626C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083664 | ||||||
| chr3:49083992
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21-6954C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083992 | ||||||
| chr3:49084380
|
A | G | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-7342T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084380 | ||||||
| chr3:49084661
|
G | A | 10 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 10 | HG00609.hp1 HG02015.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-7623C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084661 | ||||||
| chr3:49084688
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7650G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084688 | ||||||
| chr3:49084695
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-7657G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084695 | ||||||
| chr3:49084823
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-21-7785T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084823 | ||||||
| chr3:49084827
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-21-7789T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084827 | ||||||
| chr3:49085159
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-8121A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085159 | ||||||
| chr3:49085629
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-22+8283C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085629 | ||||||
| chr3:49085673
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+8239C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085673 | ||||||
| chr3:49085879
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+8033T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085879 | ||||||
| chr3:49086133
|
T | TA | 10 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 10 | HG02280.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22+7778dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086133 | ||||||
| chr3:49086204
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22+7708C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086204 | ||||||
| chr3:49086261
|
C | CT | 24 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(21): Show | 24 | HG00609.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22+7650dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086261 | ||||||
| chr3:49086261
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0074a0001c0001t0001g0151a0001c0001t0001g0154 | 3 | HG02886.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-22+7638_-22+7650d others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086261 | ||||||
| chr3:49086296
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+7616C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086296 | ||||||
| chr3:49086326
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG03490.hp2 HG03492.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-22+7586C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086326 | ||||||
| chr3:49086469
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+7443C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086469 | ||||||
| chr3:49086470
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+7442C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086470 | ||||||
| chr3:49087013
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-22+6899A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087013 | ||||||
| chr3:49087150
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-22+6762C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087150 | ||||||
| chr3:49087212
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-22+6700C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087212 | ||||||
| chr3:49087213
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-22+6699G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087213 | ||||||
| chr3:49087384
|
T | G | 32 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-22+6528A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087384 | ||||||
| chr3:49087470
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-22+6442C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087470 | ||||||
| chr3:49087630
|
C | T | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(3): Show | 6 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+6282G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087630 | ||||||
| chr3:49087728
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 9 | HG00544.hp2 HG02280.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+6184C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087728 | ||||||
| chr3:49087818
|
C | CA | 14 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0200others(11): Show | 14 | HG01515.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22+6093dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAA | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 28 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-22+6092_-22+6093d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0185 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-22+6084_-22+6093d others(12): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(4): Show |
21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0067others(18): Show | 21 | HG00140.hp2 HG00639.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-22+6083_-22+6093d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(5): Show |
35 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0099others(32): Show | 35 | HG00738.hp1 HG00738.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.-22+6082_-22+6093d others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(6): Show |
34 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0076others(31): Show | 34 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-22+6081_-22+6093d others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(7): Show |
25 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0077others(22): Show | 25 | HG01074.hp1 HG01261.hp1 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22+6080_-22+6093d others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0148a0001c0001t0001g0157others(4): Show | 7 | HG01981.hp1 HG01981.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+6079_-22+6093d others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0165others(1): Show | 4 | HG01192.hp2 HG01255.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+6078_-22+6093d others(18): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-22+6077_-22+6093d others(19): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0149 | 3 | HG00544.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-22+6076_-22+6093d others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154 | 3 | HG02886.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-22+6075_-22+6093d others(21): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087818
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22+6073_-22+6093d others(23): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | ||||||
| chr3:49087842
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-22+6070T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087842 | ||||||
| chr3:49087858
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-22+6054A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087858 | ||||||
| chr3:49087875
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-22+6037T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087875 | ||||||
| chr3:49087956
|
AT | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0153a0001c0001t0002g0003others(2): Show | 5 | HG00733.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+5955delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087956 | ||||||
| chr3:49088068
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-22+5844G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088068 | ||||||
| chr3:49088170
|
C | G | 4 | a0001c0001t0001g0218a0001c0001t0002g0003a0001c0001t0002g0219others(1): Show | 4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+5742G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088170 | ||||||
| chr3:49088219
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.-22+5693C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088219 | ||||||
| chr3:49088233
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-22+5679C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088233 | ||||||
| chr3:49088262
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+5650C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088262 | ||||||
| chr3:49088440
|
C | T | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(3): Show | 6 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+5472G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088440 | ||||||
| chr3:49088618
|
G | GT | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG00735.hp1 HG01070.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22+5293dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088618 | ||||||
| chr3:49088708
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+5204G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088708 | ||||||
| chr3:49089041
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+4871G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089041 | ||||||
| chr3:49089099
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+4813G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089099 | ||||||
| chr3:49089308
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22+4604G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089308 | ||||||
| chr3:49089368
|
A | G | 1 | a0002c0002t0001g0010 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-22+4544T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089368 | ||||||
| chr3:49089409
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22+4503A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089409 | ||||||
| chr3:49089421
|
A | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18963.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-22+4491T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089421 | ||||||
| chr3:49089817
|
T | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+4095A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089817 | ||||||
| chr3:49090197
|
C | A | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+3715G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090197 | ||||||
| chr3:49090197
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22+3715G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090197 | ||||||
| chr3:49090287
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0070 | 3 | NA19003.hp1 NA19012.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-22+3625C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090287 | ||||||
| chr3:49090453
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-22+3459G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090453 | ||||||
| chr3:49090458
|
C | CA | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.-22+3453dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090458 | ||||||
| chr3:49090458
|
C | CAA | 9 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(6): Show | 9 | HG01981.hp1 HG02074.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+3452_-22+3453d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090458 | ||||||
| chr3:49090628
|
C | CA | 111 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-22+3283dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090628 | ||||||
| chr3:49090628
|
C | CAA | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-22+3282_-22+3283d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090628 | ||||||
| chr3:49090986
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22+2926C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090986 | ||||||
| chr3:49091810
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-22+2102C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49091810 | ||||||
| chr3:49092148
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+1764C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092148 | ||||||
| chr3:49092192
|
T | C | 21 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+1720A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092192 | ||||||
| chr3:49092230
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-22+1682C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092230 | ||||||
| chr3:49092381
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG00639.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-22+1531T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092381 | ||||||
| chr3:49092626
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+1286C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092626 | ||||||
| chr3:49092642
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-22+1270G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092642 | ||||||
| chr3:49092682
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+1230T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092682 | ||||||
| chr3:49092691
|
GAACA | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-22+1217_-22+1220d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092691 | ||||||
| chr3:49092833
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-22+1079T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092833 | ||||||
| chr3:49092841
|
A | G | 1 | a0001c0001t0001g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+1071T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092841 | ||||||
| chr3:49092917
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-22+995A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092917 | ||||||
| chr3:49092945
|
T | C | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG00140.hp2 HG00280.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+967A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092945 | ||||||
| chr3:49093165
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+747C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093165 | ||||||
| chr3:49093305
|
C | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0219a0001c0004t0002g0002 | 3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+607G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093305 | ||||||
| chr3:49093820
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-22+92C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093820 | ||||||
| chr3:49093871
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-22+41G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093871 |