Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 221421 |
|---|---|
| ensemblid | ENSG00000172426.16 |
| hgncid | 21057 |
| symbol | RSPH9 |
| name | radial spoke head component 9 |
| refseq_nuc | NM_152732.5 |
| refseq_prot | NP_689945.2 |
| ensembl_nuc | ENST00000372163.5 |
| ensembl_prot | ENSP00000361236.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 43645036 |
| end | 43672600 |
| strand | + |
| ver | v1.2 |
| region | chr6:43645036-43672600 |
| region5000 | chr6:43640036-43677600 |
| regionname0 | RSPH9_chr6_43645036_43672600 |
| regionname5000 | RSPH9_chr6_43640036_43677600 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 276 | 260 | 85 | 49 | 88 | 11 | 25 | 71 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002 | 0/0 | 276 | 71 | 3 | 4 | 50 | 3 | 11 | 36 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0003 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0004 | 0/0 | 276 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0005 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0006 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 831 | 257 | 84 | 48 | 87 | 11 | 25 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0002 | 0/0 | 831 | 70 | 3 | 4 | 50 | 3 | 10 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0003 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0004 | 0/0 | 831 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0005 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0006 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0007 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0008 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0009 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| c0010 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1715 | 198 | 38 | 42 | 84 | 10 | 22 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0002 | 0/0 | 1715 | 69 | 2 | 4 | 49 | 3 | 11 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0003 | 0/0 | 1715 | 17 | 4 | 4 | 8 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0004 | 0/0 | 1715 | 10 | 10 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0005 | 0/0 | 1715 | 8 | 8 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0006 | 0/0 | 1715 | 7 | 6 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0007 | 0/0 | 1715 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0008 | 0/0 | 1715 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0009 | 0/0 | 1715 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0010 | 0/0 | 1715 | 3 | 3 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0011 | 0/0 | 1715 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0012 | 0/0 | 1715 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0013 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0014 | 0/0 | 1715 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0015 | 0/0 | 1715 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0016 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0017 | 0/0 | 1715 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0018 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0019 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0020 | 0/0 | 1715 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0021 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| t0022 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 20 | 1 | 4 | 13 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0003 | 0/0 | 6 | 0 | 0 | 3 | 2 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0028 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 831 | 257 | 84 | 48 | 87 | 11 | 25 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0007 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0008 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0009 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0002 | 0/0 | 831 | 70 | 3 | 4 | 50 | 3 | 10 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0005 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0003c0003 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0004c0004 | 0/0 | 831 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0005c0006 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0006c0010 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2545 | 189 | 34 | 41 | 80 | 10 | 22 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0003 | 0/0 | 2545 | 15 | 4 | 3 | 7 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0004 | 0/0 | 2545 | 10 | 10 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0005 | 0/0 | 2545 | 8 | 8 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0006 | 0/0 | 2545 | 7 | 6 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0007 | 0/0 | 2545 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0008 | 0/0 | 2545 | 6 | 6 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0009 | 0/0 | 2545 | 3 | 3 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0010 | 0/0 | 2545 | 3 | 3 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0011 | 0/0 | 2545 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0012 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0013 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0015 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0016 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0017 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0020 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0021 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0001t0022 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0007t0003 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0008t0012 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0001c0009t0003 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0002t0002 | 0/0 | 2545 | 68 | 2 | 4 | 49 | 3 | 10 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0002t0014 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0002t0019 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0002c0005t0002 | 0/0 | 2545 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0003c0003t0001 | 0/0 | 2545 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0003c0003t0009 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0003c0003t0018 | 0/0 | 2545 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0004c0004t0001 | 0/0 | 2545 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0005c0006t0001 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| a0006c0010t0001 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | copy fasta | chr6 | 43640036 | 43677600 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 1 | 4 | 11 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 3 | 2 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0028 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0010g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0011g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0013g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0015g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0017g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0020g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0021g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0001t0022g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0007t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0008t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0001c0009t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0014g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0002t0019g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0002c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0003c0003t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0005c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| a0006c0010t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0020 | EUR | FIN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | CHS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0209 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0138 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0012 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0012 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0085 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01516 | hp1 | a0001 | c0001 | t0020 | g0109 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0086 | EUR | IBS | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01993 | hp1 | a0001 | c0009 | t0003 | g0220 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0010 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | CDX | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02258 | hp2 | a0003 | c0003 | t0018 | g0064 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0099 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0098 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0251 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02723 | hp1 | a0001 | c0008 | t0012 | g0247 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02738 | hp1 | a0001 | c0001 | t0015 | g0198 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02809 | hp2 | a0002 | c0002 | t0019 | g0081 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0248 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02965 | hp2 | a0003 | c0003 | t0009 | g0062 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0097 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03688 | hp2 | a0002 | c0005 | t0002 | g0094 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0134 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0237 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0083 | SAS | STU | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18951 | hp1 | a0001 | c0007 | t0003 | g0224 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18957 | hp2 | a0004 | c0004 | t0001 | g0167 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18984 | hp2 | a0005 | c0006 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0226 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0065 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19088 | hp1 | a0002 | c0002 | t0014 | g0203 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ASW | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG01123 | hp2 | a0006 | c0010 | t0001 | g0183 | AMR | CLM | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0262 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0174 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | LWK | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0028 | REF | REF | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | RSPH9_chr6_43640036_43677600 | RSPH9 | chr6 | 43640036 | 43677600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645109
|
A | G | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.11A>G | p.Asp4Gly | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 74/2545 | 11/831 | 4/276 | chr6 | 43645109 | ||
| chr6:43650410
|
C | T | 1 | a0003 | 6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
missense_variant | MODERATE | c.263C>T | p.Ala88Val | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/5 | 326/2545 | 263/831 | 88/276 | chr6 | 43650410 | ||
| chr6:43655589
|
G | A | 1 | a0004 | 3 | HG02056.hp2 NA18946.hp1 NA18957.hp2 |
missense_variant | MODERATE | c.421G>A | p.Val141Met | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/5 | 484/2545 | 421/831 | 141/276 | chr6 | 43655589 | ||
| chr6:43655640
|
G | A | 1 | a0005 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.472G>A | p.Ala158Thr | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/5 | 535/2545 | 472/831 | 158/276 | chr6 | 43655640 | ||
| chr6:43670899
|
G | A | 1 | a0002 | 71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
missense_variant | MODERATE | c.781G>A | p.Val261Ile | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 844/2545 | 781/831 | 261/276 | chr6 | 43670899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645227
|
G | A | 1 | a0002c0005 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.129G>A | p.Arg43Arg | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 192/2545 | 129/831 | 43/276 | chr6 | 43645227 | ||
| chr6:43656579
|
C | T | 1 | a0001c0009 | 1 | HG01993.hp1 | splice_region_variant&synonymous_variant | LOW | c.526C>T | p.Leu176Leu | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/5 | 589/2545 | 526/831 | 176/276 | chr6 | 43656579 | ||
| chr6:43670898
|
C | T | 1 | a0001c0008 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.780C>T | p.Tyr260Tyr | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 843/2545 | 780/831 | 260/276 | chr6 | 43670898 | ||
| chr6:43670937
|
C | T | 1 | a0001c0007 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.819C>T | p.Pro273Pro | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 882/2545 | 819/831 | 273/276 | chr6 | 43670937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645081
|
A | G | 5 | a0001c0001t0008a0001c0001t0010a0001c0001t0012others(2): Show | 12 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-18A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/5 | 18 | chr6 | 43645081 | |||||
| chr6:43671279
|
T | C | 2 | a0001c0001t0007a0001c0001t0022 | 7 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 330 | chr6 | 43671279 | |||||
| chr6:43671363
|
C | T | 1 | a0001c0001t0021 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 414 | chr6 | 43671363 | |||||
| chr6:43671375
|
G | A | 1 | a0001c0001t0013 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 426 | chr6 | 43671375 | |||||
| chr6:43671437
|
A | G | 1 | a0001c0001t0020 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 488 | chr6 | 43671437 | |||||
| chr6:43671483
|
C | T | 1 | a0001c0001t0021 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 534 | chr6 | 43671483 | |||||
| chr6:43671726
|
C | G | 1 | a0001c0001t0005 | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 777 | chr6 | 43671726 | |||||
| chr6:43671781
|
G | C | 1 | a0002c0002t0014 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 832 | chr6 | 43671781 | |||||
| chr6:43671896
|
G | A | 1 | a0001c0001t0015 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*947G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 947 | chr6 | 43671896 | |||||
| chr6:43671971
|
G | A | 2 | a0001c0001t0004a0001c0001t0016 | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1022G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1022 | chr6 | 43671971 | |||||
| chr6:43671995
|
C | T | 1 | a0002c0002t0019 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1046 | chr6 | 43671995 | |||||
| chr6:43672117
|
G | A | 1 | a0001c0001t0016 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1168G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1168 | chr6 | 43672117 | |||||
| chr6:43672141
|
G | T | 2 | a0001c0001t0008a0003c0003t0018 | 7 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1192G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1192 | chr6 | 43672141 | |||||
| chr6:43672149
|
C | T | 7 | a0001c0001t0003a0001c0007t0003a0001c0009t0003others(4): Show | 88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1200 | chr6 | 43672149 | |||||
| chr6:43672302
|
C | T | 7 | a0001c0001t0003a0001c0007t0003a0001c0009t0003others(4): Show | 88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1353 | chr6 | 43672302 | |||||
| chr6:43672327
|
A | G | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(7): Show | 104 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1378A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1378 | chr6 | 43672327 | |||||
| chr6:43672360
|
G | A | 1 | a0001c0001t0017 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1411 | chr6 | 43672360 | |||||
| chr6:43672362
|
A | G | 7 | a0001c0001t0003a0001c0007t0003a0001c0009t0003others(4): Show | 88 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1413 | chr6 | 43672362 | |||||
| chr6:43672441
|
G | T | 3 | a0001c0001t0009a0001c0001t0010a0003c0003t0009 | 7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1492G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1492 | chr6 | 43672441 | |||||
| chr6:43672485
|
A | G | 4 | a0001c0001t0003a0001c0001t0011a0001c0007t0003others(1): Show | 19 | HG01074.hp2 HG01099.hp1 HG01257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1536A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 5/5 | 1536 | chr6 | 43672485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43645367
|
C | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0260a0001c0001t0004g0258others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+42C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645367 | ||||||
| chr6:43645408
|
G | A | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.227+83G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645408 | ||||||
| chr6:43645443
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 36 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.227+118G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645443 | ||||||
| chr6:43645591
|
T | TC | 28 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0076others(25): Show | 29 | HG00639.hp2 HG01175.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.227+271dupC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43645591 | |||||
| chr6:43645591
|
TC | T | 19 | a0001c0001t0001g0036a0001c0001t0001g0250a0001c0001t0001g0255others(16): Show | 20 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.227+271delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43645591 | |||||
| chr6:43645613
|
C | A | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+288C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645613 | ||||||
| chr6:43645653
|
A | T | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.227+328A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645653 | ||||||
| chr6:43645928
|
T | C | 1 | a0002c0002t0002g0089 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.227+603T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43645928 | ||||||
| chr6:43646125
|
TTTATTA | T | 7 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(4): Show | 7 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+818_227+823del others(6): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646125 | |||||
| chr6:43646128
|
A | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.227+803A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646128 | ||||||
| chr6:43646242
|
C | G | 7 | a0001c0001t0001g0033a0001c0001t0001g0228a0001c0001t0001g0230others(4): Show | 8 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+917C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646242 | ||||||
| chr6:43646328
|
G | T | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.227+1003G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646328 | ||||||
| chr6:43646336
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0232a0001c0001t0001g0233 | 5 | NA18747.hp1 NA18974.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.227+1011G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646336 | ||||||
| chr6:43646468
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.227+1143G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646468 | ||||||
| chr6:43646496
|
C | T | 7 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01978.hp2 HG01993.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.227+1171C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646496 | ||||||
| chr6:43646570
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.227+1245C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646570 | ||||||
| chr6:43646664
|
C | CA | 24 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(21): Show | 28 | HG00738.hp1 HG01192.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.227+1355dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646664 | |||||
| chr6:43646664
|
C | CAA | 11 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0004g0066others(8): Show | 11 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.227+1354_227+1355d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646664 | |||||
| chr6:43646687
|
GTGTGGTG others(25): Show |
G | 1 | a0001c0001t0001g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.227+1365_227+1396d others(34): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646687 | |||||
| chr6:43646776
|
C | T | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.227+1451C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646776 | ||||||
| chr6:43646829
|
G | A | 1 | a0003c0003t0009g0062 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.227+1504G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646829 | ||||||
| chr6:43646863
|
G | A | 2 | a0001c0001t0004g0074a0001c0001t0006g0073 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.227+1538G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646863 | ||||||
| chr6:43646930
|
G | C | 6 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(3): Show | 6 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.227+1605G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646930 | ||||||
| chr6:43646949
|
C | G | 3 | a0001c0001t0001g0036a0001c0001t0005g0253a0001c0001t0006g0037 | 4 | HG02895.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.227+1624C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646949 | ||||||
| chr6:43646954
|
CA | C | 7 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0230others(4): Show | 7 | HG01255.hp1 NA18942.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+1642delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646954 | |||||
| chr6:43646968
|
G | A | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+1643G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646968 | ||||||
| chr6:43646968
|
GA | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(74): Show | 91 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.227+1654delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43646968 | |||||
| chr6:43646969
|
A | G | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227+1644A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43646969 | ||||||
| chr6:43647077
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(68): Show | 85 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.227+1752A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647077 | ||||||
| chr6:43647095
|
G | A | 4 | a0003c0003t0001g0063a0003c0003t0001g0065a0003c0003t0009g0062others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.227+1770G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647095 | ||||||
| chr6:43647109
|
ACAGAGCG others(58): Show |
A | 5 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 8 | HG00140.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+1788_227+1852d others(67): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43647109 | |||||
| chr6:43647182
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.227+1857G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647182 | ||||||
| chr6:43647359
|
C | A | 8 | a0001c0001t0001g0102a0001c0001t0008g0006a0001c0001t0008g0100others(5): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.227+2034C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647359 | ||||||
| chr6:43647407
|
G | A | 3 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0005g0068 | 3 | HG02615.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.227+2082G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647407 | ||||||
| chr6:43647697
|
A | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.227+2372A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647697 | ||||||
| chr6:43647890
|
C | T | 18 | a0001c0001t0001g0036a0001c0001t0001g0250a0001c0001t0001g0255others(15): Show | 19 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.228-2485C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647890 | ||||||
| chr6:43647904
|
C | T | 25 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(22): Show | 30 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.228-2471C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647904 | ||||||
| chr6:43647933
|
A | T | 5 | a0001c0001t0004g0074a0001c0001t0005g0079a0001c0001t0005g0080others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-2442A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647933 | ||||||
| chr6:43647999
|
G | A | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.228-2376G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43647999 | ||||||
| chr6:43648223
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0004g0104 | 3 | NA19043.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.228-2152C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648223 | ||||||
| chr6:43648269
|
C | CA | 10 | a0001c0001t0001g0070a0001c0001t0004g0066a0001c0001t0004g0067others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.228-2092dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43648269 | |||||
| chr6:43648283
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-2092A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648283 | ||||||
| chr6:43648451
|
T | A | 1 | a0002c0002t0002g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.228-1924T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648451 | ||||||
| chr6:43648865
|
G | A | 4 | a0001c0001t0004g0074a0001c0001t0005g0079a0001c0001t0005g0080others(1): Show | 4 | HG02486.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1510G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648865 | ||||||
| chr6:43648890
|
G | A | 7 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(4): Show | 7 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1485G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43648890 | ||||||
| chr6:43649055
|
T | C | 1 | a0001c0001t0003g0108 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.228-1320T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649055 | ||||||
| chr6:43649194
|
T | G | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.228-1181T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649194 | ||||||
| chr6:43649258
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228-1117C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649258 | ||||||
| chr6:43649266
|
T | G | 15 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0260others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.228-1109T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649266 | ||||||
| chr6:43649412
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 8 | HG02486.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.228-963G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649412 | ||||||
| chr6:43649466
|
C | T | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-909C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649466 | ||||||
| chr6:43649496
|
T | C | 1 | a0002c0002t0002g0009 | 3 | NA18747.hp2 NA18945.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.228-879T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649496 | ||||||
| chr6:43649571
|
T | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 7 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-804T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649571 | ||||||
| chr6:43649643
|
G | A | 1 | a0001c0001t0017g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.228-732G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649643 | ||||||
| chr6:43649817
|
A | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(71): Show | 88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-558A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649817 | ||||||
| chr6:43649850
|
TCATTTAA others(6): Show |
T | 1 | a0001c0001t0020g0109 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.228-521_228-509del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 43649850 | |||||
| chr6:43649950
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.228-425G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649950 | ||||||
| chr6:43649972
|
G | A | 1 | a0002c0002t0019g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228-403G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649972 | ||||||
| chr6:43649978
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(71): Show | 88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-397G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649978 | ||||||
| chr6:43649989
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.228-386C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43649989 | ||||||
| chr6:43650258
|
A | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.228-117A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650258 | ||||||
| chr6:43650273
|
C | T | 6 | a0001c0001t0001g0250a0001c0001t0003g0249a0001c0001t0004g0252others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-102C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650273 | ||||||
| chr6:43650289
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(71): Show | 88 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(85): Show |
intron_variant | MODIFIER | c.228-86C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 1/4 | chr6 | 43650289 | ||||||
| chr6:43650634
|
C | T | 2 | a0001c0001t0006g0209a0001c0001t0006g0210 | 2 | HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.393+94C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650634 | ||||||
| chr6:43650639
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.393+99G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650639 | ||||||
| chr6:43650694
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.393+154C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650694 | ||||||
| chr6:43650734
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.393+194G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650734 | ||||||
| chr6:43650760
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0004g0074a0001c0001t0005g0079others(2): Show | 5 | HG02486.hp1 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+220G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650760 | ||||||
| chr6:43650860
|
G | A | 1 | a0001c0001t0004g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+320G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43650860 | ||||||
| chr6:43650905
|
T | TA | 61 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(58): Show | 75 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.393+379dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650905 | |||||
| chr6:43650905
|
T | TAA | 15 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0260others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+378_393+379dup others(2): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650905 | |||||
| chr6:43650947
|
CA | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+409delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43650947 | |||||
| chr6:43651118
|
G | A | 1 | a0001c0001t0022g0097 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.393+578G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651118 | ||||||
| chr6:43651311
|
G | A | 6 | a0001c0001t0001g0250a0001c0001t0003g0249a0001c0001t0004g0252others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+771G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651311 | ||||||
| chr6:43651441
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0005g0253a0001c0001t0006g0037 | 4 | HG02895.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+901G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651441 | ||||||
| chr6:43651489
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+949T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651489 | ||||||
| chr6:43651546
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.393+1006T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651546 | ||||||
| chr6:43651633
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0096 | 3 | HG01192.hp2 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.393+1093C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651633 | ||||||
| chr6:43651700
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0070others(41): Show | 54 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+1160T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651700 | ||||||
| chr6:43651756
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.393+1216C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651756 | ||||||
| chr6:43651828
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.393+1288C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651828 | ||||||
| chr6:43651845
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(46): Show | 62 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.393+1305A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651845 | ||||||
| chr6:43651914
|
T | A | 1 | a0002c0002t0002g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.393+1374T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651914 | ||||||
| chr6:43651942
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.393+1402T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651942 | ||||||
| chr6:43651994
|
T | A | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+1454T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43651994 | ||||||
| chr6:43652261
|
G | A | 2 | a0001c0001t0005g0253a0001c0001t0006g0037 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.393+1721G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652261 | ||||||
| chr6:43652285
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+1745G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652285 | ||||||
| chr6:43652373
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.393+1833C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652373 | ||||||
| chr6:43652406
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+1866G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652406 | ||||||
| chr6:43652464
|
C | T | 1 | a0002c0002t0014g0203 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.393+1924C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652464 | ||||||
| chr6:43652519
|
G | A | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.393+1979G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652519 | ||||||
| chr6:43652643
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.393+2103C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652643 | ||||||
| chr6:43652661
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.393+2121G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652661 | ||||||
| chr6:43652672
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.393+2132C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652672 | ||||||
| chr6:43652728
|
CG | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0217others(11): Show | 14 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+2190delG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652728 | |||||
| chr6:43652729
|
GGT | G | 9 | a0001c0001t0001g0105a0001c0001t0003g0082a0001c0001t0004g0104others(6): Show | 13 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.393+2190_393+2191d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652729 | ||||||
| chr6:43652730
|
G | GT | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 114 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.393+2207dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | |||||
| chr6:43652730
|
G | GTT | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02738.hp1 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2206_393+2207d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | |||||
| chr6:43652730
|
GT | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0033others(32): Show | 45 | HG00642.hp2 HG01081.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.393+2207delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43652730 | |||||
| chr6:43652807
|
C | T | 3 | a0001c0001t0004g0252a0001c0001t0007g0254a0001c0001t0016g0251 | 3 | HG02717.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.393+2267C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652807 | ||||||
| chr6:43652808
|
G | A | 1 | a0002c0002t0002g0075 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.393+2268G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652808 | ||||||
| chr6:43652818
|
T | A | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.393+2278T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652818 | ||||||
| chr6:43652903
|
C | A | 2 | a0001c0001t0005g0253a0001c0001t0006g0037 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.393+2363C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43652903 | ||||||
| chr6:43653008
|
T | TG | 15 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0004g0074others(12): Show | 16 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.393+2472dupG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653008 | |||||
| chr6:43653095
|
T | C | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2467T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653095 | ||||||
| chr6:43653153
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0004g0104 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.394-2409A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653153 | ||||||
| chr6:43653259
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.394-2303G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653259 | ||||||
| chr6:43653279
|
G | A | 1 | a0002c0002t0002g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.394-2283G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653279 | ||||||
| chr6:43653371
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(15): Show | 26 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.394-2191C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653371 | ||||||
| chr6:43653379
|
G | A | 6 | a0003c0003t0001g0063a0003c0003t0001g0065a0003c0003t0001g0069others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-2183G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653379 | ||||||
| chr6:43653401
|
C | T | 1 | a0002c0002t0002g0216 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.394-2161C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653401 | ||||||
| chr6:43653409
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0106a0001c0001t0001g0156others(3): Show | 9 | HG00597.hp1 NA18940.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-2153T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653409 | ||||||
| chr6:43653434
|
A | G | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2128A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653434 | ||||||
| chr6:43653441
|
C | T | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-2121C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653441 | ||||||
| chr6:43653446
|
C | CA | 26 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0091others(23): Show | 27 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-2097dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | |||||
| chr6:43653446
|
C | CAA | 19 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0105others(16): Show | 23 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.394-2098_394-2097d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | |||||
| chr6:43653446
|
CA | C | 8 | a0001c0001t0001g0061a0001c0001t0001g0102a0001c0001t0001g0193others(5): Show | 8 | HG01256.hp2 HG02257.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-2097delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | |||||
| chr6:43653446
|
CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0042others(7): Show | 12 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-2105_394-2097d others(11): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653446 | |||||
| chr6:43653469
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.394-2093C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653469 | ||||||
| chr6:43653489
|
T | TGTGTGTA others(9): Show |
1 | a0001c0001t0001g0202 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.394-2072_394-2057d others(18): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 43653489 | |||||
| chr6:43653532
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-2030C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653532 | ||||||
| chr6:43653586
|
AAGCACAG others(3): Show |
A | 1 | a0001c0007t0003g0224 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.394-1975_394-1966d others(12): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653586 | ||||||
| chr6:43653748
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.394-1814A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653748 | ||||||
| chr6:43653788
|
A | G | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1774A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653788 | ||||||
| chr6:43653872
|
G | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(72): Show | 89 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.394-1690G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653872 | ||||||
| chr6:43653904
|
T | C | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1658T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43653904 | ||||||
| chr6:43654177
|
G | C | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394-1385G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654177 | ||||||
| chr6:43654188
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-1374G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654188 | ||||||
| chr6:43654238
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394-1324A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654238 | ||||||
| chr6:43654302
|
A | G | 24 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(21): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-1260A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654302 | ||||||
| chr6:43654516
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0004g0074a0001c0001t0005g0079others(3): Show | 6 | HG02486.hp1 HG02809.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-1046C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654516 | ||||||
| chr6:43654548
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0029others(24): Show | 37 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.394-1014C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654548 | ||||||
| chr6:43654549
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 8 | HG00140.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-1013G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654549 | ||||||
| chr6:43654695
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.394-867C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654695 | ||||||
| chr6:43654763
|
C | T | 6 | a0003c0003t0001g0063a0003c0003t0001g0065a0003c0003t0001g0069others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-799C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654763 | ||||||
| chr6:43654783
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-779A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43654783 | ||||||
| chr6:43655019
|
A | G | 6 | a0001c0001t0005g0032a0001c0001t0005g0079a0001c0001t0005g0080others(3): Show | 7 | HG02257.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-543A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655019 | ||||||
| chr6:43655064
|
T | C | 16 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0102others(13): Show | 16 | HG01106.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-498T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655064 | ||||||
| chr6:43655099
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.394-463A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655099 | ||||||
| chr6:43655118
|
G | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0029others(120): Show | 159 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.394-444G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655118 | ||||||
| chr6:43655188
|
A | G | 38 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0117others(35): Show | 38 | HG00597.hp2 HG00639.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.394-374A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655188 | ||||||
| chr6:43655217
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.394-345C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655217 | ||||||
| chr6:43655365
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(14): Show | 25 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.394-197C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655365 | ||||||
| chr6:43655377
|
C | T | 83 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0117others(80): Show | 103 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.394-185C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655377 | ||||||
| chr6:43655392
|
G | T | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-170G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655392 | ||||||
| chr6:43655405
|
A | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0034others(49): Show | 65 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(62): Show |
intron_variant | MODIFIER | c.394-157A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655405 | ||||||
| chr6:43655406
|
T | C | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-156T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655406 | ||||||
| chr6:43655537
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0004g0188 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.394-25G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 2/4 | chr6 | 43655537 | ||||||
| chr6:43655786
|
C | T | 1 | a0002c0005t0002g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.523+95C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655786 | ||||||
| chr6:43655911
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0049 | 4 | HG00140.hp1 HG01192.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+220A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655911 | ||||||
| chr6:43655988
|
A | ACTTC | 17 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0033others(14): Show | 24 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.523+343_523+346dup others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655988
|
A | ACTTCCTT others(1): Show |
27 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(24): Show | 32 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.523+339_523+346dup others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655988
|
A | ACTTCCTT others(5): Show |
7 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0060others(4): Show | 7 | HG01256.hp2 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+335_523+346dup others(12): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655988
|
A | ACTTCCTT others(9): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0151a0001c0001t0011g0012 | 5 | HG01257.hp2 HG01258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+331_523+346dup others(16): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655988
|
A | ACTTCCTT others(13): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.523+327_523+346dup others(20): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655988
|
ACTTC | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0031others(15): Show | 21 | HG00280.hp1 HG01192.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.523+343_523+346del others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43655988 | |||||
| chr6:43655992
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.523+301C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655992 | ||||||
| chr6:43655992
|
C | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(55): Show | 72 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.523+301C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43655992 | ||||||
| chr6:43656028
|
CCTTCCTT others(10): Show |
C | 23 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(20): Show | 34 | HG00642.hp2 HG01884.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.523+339_523+355del others(17): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656028 | |||||
| chr6:43656032
|
CCTTCCCC others(6): Show |
C | 11 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0137others(8): Show | 14 | HG01081.hp2 HG01106.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.523+343_523+355del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656032 | |||||
| chr6:43656034
|
T | G | 3 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0236 | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+343T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656034 | ||||||
| chr6:43656035
|
TC | T | 30 | a0001c0001t0001g0129a0001c0001t0001g0148a0001c0001t0001g0260others(27): Show | 42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+348delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656035 | |||||
| chr6:43656036
|
C | CCTTCCTT others(4): Show |
2 | a0001c0001t0001g0048a0001c0001t0020g0109 | 2 | HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.523+346_523+347ins others(11): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | |||||
| chr6:43656036
|
CCCCTT | C | 20 | a0001c0001t0001g0105a0001c0001t0001g0147a0001c0001t0005g0079others(17): Show | 23 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+347_523+351del others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | |||||
| chr6:43656036
|
CCCCTTCT others(2): Show |
C | 8 | a0001c0001t0001g0102a0001c0001t0004g0074a0001c0001t0004g0104others(5): Show | 9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.523+368_523+376del others(9): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656036 | |||||
| chr6:43656037
|
C | CTT | 20 | a0001c0001t0001g0103a0001c0001t0001g0217a0001c0001t0007g0261others(17): Show | 23 | HG00621.hp1 HG00639.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+346_523+347ins others(2): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | ||||||
| chr6:43656037
|
C | CTTCCTT | 7 | a0001c0001t0007g0256a0001c0001t0007g0257a0001c0001t0007g0262others(4): Show | 8 | HG02109.hp2 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+346_523+347ins others(6): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | ||||||
| chr6:43656037
|
C | CTTCCTTC others(3): Show |
3 | a0001c0001t0004g0252a0001c0001t0007g0254a0002c0002t0002g0136 | 3 | HG02683.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.523+346_523+347ins others(10): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | ||||||
| chr6:43656037
|
C | CTTCCTTC others(10): Show |
1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.523+346_523+347ins others(17): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656037 | ||||||
| chr6:43656038
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0112 | 2 | HG01346.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.523+347C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656038 | ||||||
| chr6:43656039
|
C | T | 30 | a0001c0001t0001g0129a0001c0001t0001g0148a0001c0001t0001g0260others(27): Show | 42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+348C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656039 | ||||||
| chr6:43656041
|
T | C | 30 | a0001c0001t0001g0129a0001c0001t0001g0148a0001c0001t0001g0260others(27): Show | 42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.523+350T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656041 | ||||||
| chr6:43656041
|
T | TC | 27 | a0001c0001t0001g0103a0001c0001t0001g0217a0001c0001t0004g0252others(24): Show | 31 | HG00621.hp1 HG02109.hp2 HG02273.hp2 others(28): Show |
intron_variant | MODIFIER | c.523+351dupC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656041 | |||||
| chr6:43656043
|
T | C | 4 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0087others(1): Show | 4 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+352T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656043 | ||||||
| chr6:43656043
|
T | G | 4 | a0001c0001t0005g0079a0001c0001t0005g0080a0001c0001t0005g0253others(1): Show | 4 | HG02965.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+352T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656043 | ||||||
| chr6:43656045
|
T | C | 77 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0129others(74): Show | 96 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.523+354T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656045 | ||||||
| chr6:43656048
|
C | T | 5 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+357C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656048 | ||||||
| chr6:43656050
|
T | C | 5 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+359T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656050 | ||||||
| chr6:43656054
|
T | C | 6 | a0001c0001t0001g0117a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+363T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656054 | ||||||
| chr6:43656057
|
CTTCTTTC others(6): Show |
C | 1 | a0003c0003t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.523+368_523+380del others(13): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656057 | |||||
| chr6:43656070
|
TTCCC | T | 6 | a0002c0002t0002g0088a0003c0003t0001g0065a0003c0003t0001g0069others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.523+397_523+400del others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 43656070 | |||||
| chr6:43656074
|
C | T | 1 | a0003c0003t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.523+383C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656074 | ||||||
| chr6:43656093
|
T | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(104): Show | 141 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.523+402T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656093 | ||||||
| chr6:43656108
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0034others(13): Show | 23 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+417G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656108 | ||||||
| chr6:43656121
|
T | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0034others(34): Show | 48 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.523+430T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656121 | ||||||
| chr6:43656129
|
A | C | 1 | a0002c0002t0002g0054 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.523+438A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656129 | ||||||
| chr6:43656221
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(31): Show | 47 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.524-356G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656221 | ||||||
| chr6:43656242
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.524-335C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656242 | ||||||
| chr6:43656280
|
T | G | 1 | a0002c0002t0002g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.524-297T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656280 | ||||||
| chr6:43656314
|
G | A | 13 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0108others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.524-263G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656314 | ||||||
| chr6:43656348
|
A | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(37): Show | 53 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.524-229A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656348 | ||||||
| chr6:43656398
|
T | C | 1 | a0002c0002t0002g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.524-179T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656398 | ||||||
| chr6:43656413
|
C | T | 6 | a0001c0001t0001g0105a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG00741.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-164C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 3/4 | chr6 | 43656413 | ||||||
| chr6:43656996
|
G | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0212 | 3 | NA18942.hp2 NA18997.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.670+273G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43656996 | ||||||
| chr6:43657057
|
A | G | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+334A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657057 | ||||||
| chr6:43657248
|
C | T | 7 | a0001c0001t0001g0143a0001c0001t0008g0006a0001c0001t0008g0100others(4): Show | 11 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+525C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657248 | ||||||
| chr6:43657286
|
G | T | 45 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(42): Show | 65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.670+563G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657286 | ||||||
| chr6:43657308
|
T | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(33): Show | 49 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.670+585T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657308 | ||||||
| chr6:43657514
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.670+791C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657514 | ||||||
| chr6:43657566
|
C | T | 46 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(43): Show | 66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+843C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657566 | ||||||
| chr6:43657569
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.670+846T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657569 | ||||||
| chr6:43657701
|
T | C | 1 | a0001c0001t0007g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.670+978T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657701 | ||||||
| chr6:43657817
|
C | T | 5 | a0001c0001t0001g0105a0001c0001t0006g0207a0001c0001t0006g0208others(2): Show | 5 | HG00741.hp1 HG02630.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+1094C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43657817 | ||||||
| chr6:43658155
|
T | C | 46 | a0001c0001t0001g0129a0001c0001t0003g0082a0002c0002t0002g0002others(43): Show | 66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+1432T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658155 | ||||||
| chr6:43658276
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.670+1553C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658276 | ||||||
| chr6:43658291
|
CAA | C | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1586_670+1587d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43658291 | |||||
| chr6:43658303
|
A | AG | 66 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(63): Show | 80 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.670+1580_670+1581i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658303 | ||||||
| chr6:43658311
|
G | A | 52 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0003g0082others(49): Show | 72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+1588G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658311 | ||||||
| chr6:43658312
|
A | AG | 13 | a0001c0001t0001g0117a0002c0002t0002g0085a0002c0002t0002g0086others(10): Show | 13 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+1589_670+1590i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658312 | ||||||
| chr6:43658312
|
A | G | 38 | a0001c0001t0001g0129a0001c0001t0003g0082a0002c0002t0002g0002others(35): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.670+1589A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658312 | ||||||
| chr6:43658360
|
C | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(123): Show | 160 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.670+1637C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658360 | ||||||
| chr6:43658389
|
G | A | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.670+1666G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658389 | ||||||
| chr6:43658396
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(21): Show | 36 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.670+1673A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658396 | ||||||
| chr6:43658471
|
T | C | 1 | a0002c0005t0002g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.670+1748T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658471 | ||||||
| chr6:43658601
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0006g0037 | 2 | HG02965.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.670+1878C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658601 | ||||||
| chr6:43658686
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.670+1963C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658686 | ||||||
| chr6:43658810
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670+2087C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43658810 | ||||||
| chr6:43659167
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.670+2444T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659167 | ||||||
| chr6:43659202
|
G | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(63): Show | 80 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.670+2479G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659202 | ||||||
| chr6:43659225
|
C | CT | 41 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(38): Show | 54 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.670+2515dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659225 | |||||
| chr6:43659225
|
C | CTT | 28 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0147others(25): Show | 29 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.670+2514_670+2515d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659225 | |||||
| chr6:43659371
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0101 | 5 | HG02258.hp1 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+2648G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659371 | ||||||
| chr6:43659386
|
C | CT | 8 | a0001c0001t0001g0031a0001c0001t0001g0096a0001c0001t0001g0139others(5): Show | 9 | HG00621.hp1 HG01192.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+2677dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43659386 | |||||
| chr6:43659414
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.670+2691G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659414 | ||||||
| chr6:43659678
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.670+2955G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659678 | ||||||
| chr6:43659944
|
C | T | 1 | a0001c0001t0011g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.670+3221C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659944 | ||||||
| chr6:43659961
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.670+3238C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659961 | ||||||
| chr6:43659983
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.670+3260G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43659983 | ||||||
| chr6:43660015
|
G | A | 16 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0082others(13): Show | 18 | HG01074.hp2 HG01099.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.670+3292G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660015 | ||||||
| chr6:43660039
|
C | CT | 26 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(23): Show | 26 | HG01192.hp1 HG01358.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+3338dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | |||||
| chr6:43660039
|
C | CTT | 51 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0005g0032others(48): Show | 72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+3337_670+3338d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | |||||
| chr6:43660039
|
C | CTTT | 6 | a0002c0002t0002g0088a0002c0002t0002g0121a0002c0002t0002g0122others(3): Show | 6 | HG01123.hp1 HG02071.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3336_670+3338d others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | |||||
| chr6:43660039
|
CTTTTTT | C | 11 | a0001c0001t0001g0102a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3333_670+3338d others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | |||||
| chr6:43660039
|
CTTTTTTT | C | 5 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0010g0017others(2): Show | 6 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3332_670+3338d others(9): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660039 | |||||
| chr6:43660192
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(56): Show | 72 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+3469G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660192 | ||||||
| chr6:43660495
|
G | A | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+3772G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660495 | ||||||
| chr6:43660594
|
G | T | 1 | a0001c0001t0017g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670+3871G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660594 | ||||||
| chr6:43660609
|
G | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(56): Show | 72 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+3886G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660609 | ||||||
| chr6:43660636
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.670+3913T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660636 | ||||||
| chr6:43660686
|
A | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(56): Show | 72 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+3963A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660686 | ||||||
| chr6:43660774
|
A | G | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.670+4051A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660774 | ||||||
| chr6:43660831
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.670+4108C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660831 | ||||||
| chr6:43660833
|
C | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(56): Show | 72 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(69): Show |
intron_variant | MODIFIER | c.670+4110C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660833 | ||||||
| chr6:43660889
|
TA | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+4171delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43660889 | |||||
| chr6:43660894
|
A | C | 1 | a0002c0002t0002g0054 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670+4171A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660894 | ||||||
| chr6:43660937
|
G | A | 11 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0074others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+4214G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660937 | ||||||
| chr6:43660979
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.670+4256C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660979 | ||||||
| chr6:43660995
|
C | G | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.670+4272C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43660995 | ||||||
| chr6:43661342
|
A | T | 1 | a0002c0002t0002g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.670+4619A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661342 | ||||||
| chr6:43661356
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01256.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.670+4633A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661356 | ||||||
| chr6:43661398
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0177a0001c0001t0001g0250 | 3 | HG01243.hp2 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.670+4675C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661398 | ||||||
| chr6:43661427
|
G | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+4704G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661427 | ||||||
| chr6:43661436
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+4713G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661436 | ||||||
| chr6:43661486
|
C | T | 12 | a0001c0001t0001g0055a0001c0001t0004g0066a0001c0001t0004g0067others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.670+4763C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661486 | ||||||
| chr6:43661489
|
C | T | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+4766C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661489 | ||||||
| chr6:43661518
|
G | A | 6 | a0001c0001t0001g0117a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+4795G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661518 | ||||||
| chr6:43661538
|
G | A | 1 | a0002c0002t0002g0054 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.670+4815G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661538 | ||||||
| chr6:43661567
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.670+4844A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661567 | ||||||
| chr6:43661653
|
T | A | 46 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(43): Show | 66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.670+4930T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661653 | ||||||
| chr6:43661653
|
T | C | 1 | a0001c0001t0013g0138 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.670+4930T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661653 | ||||||
| chr6:43661660
|
C | CA | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 165 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.670+4958dupA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | |||||
| chr6:43661660
|
C | CAA | 28 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0042others(25): Show | 30 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.670+4957_670+4958d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | |||||
| chr6:43661660
|
CA | C | 27 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0147others(24): Show | 27 | HG01934.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.670+4958delA | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43661660 | |||||
| chr6:43661759
|
G | A | 1 | a0001c0001t0017g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670+5036G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661759 | ||||||
| chr6:43661759
|
G | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0049 | 4 | HG00140.hp1 HG01192.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+5036G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661759 | ||||||
| chr6:43661809
|
G | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+5086G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661809 | ||||||
| chr6:43661811
|
A | G | 1 | a0001c0001t0004g0258 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670+5088A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661811 | ||||||
| chr6:43661948
|
C | T | 47 | a0001c0001t0001g0129a0001c0001t0001g0217a0002c0002t0002g0002others(44): Show | 67 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.670+5225C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43661948 | ||||||
| chr6:43662064
|
G | A | 45 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(42): Show | 65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.670+5341G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662064 | ||||||
| chr6:43662080
|
A | G | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.670+5357A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662080 | ||||||
| chr6:43662269
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.670+5546T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662269 | ||||||
| chr6:43662370
|
C | CTT | 44 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(41): Show | 64 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.670+5660_670+5661d others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662370 | |||||
| chr6:43662370
|
CT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0058others(10): Show | 14 | HG00140.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.670+5661delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662370 | |||||
| chr6:43662380
|
T | C | 11 | a0001c0001t0001g0102a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+5657T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662380 | ||||||
| chr6:43662658
|
C | T | 4 | a0002c0002t0002g0113a0002c0002t0002g0155a0002c0002t0002g0211others(1): Show | 4 | HG00621.hp1 NA18945.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+5935C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662658 | ||||||
| chr6:43662823
|
G | T | 16 | a0001c0001t0001g0102a0001c0001t0001g0147a0001c0001t0001g0148others(13): Show | 17 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+6100G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662823 | ||||||
| chr6:43662940
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.670+6217C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662940 | ||||||
| chr6:43662954
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(55): Show | 71 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+6231G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43662954 | ||||||
| chr6:43662968
|
A | AT | 116 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(113): Show | 150 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.670+6255dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43662968 | |||||
| chr6:43663018
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+6295A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663018 | ||||||
| chr6:43663065
|
T | C | 16 | a0001c0001t0001g0102a0001c0001t0001g0147a0001c0001t0001g0148others(13): Show | 17 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+6342T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663065 | ||||||
| chr6:43663227
|
AT | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+6513delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43663227 | |||||
| chr6:43663352
|
G | A | 1 | a0002c0002t0002g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.670+6629G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663352 | ||||||
| chr6:43663510
|
C | T | 1 | a0002c0002t0002g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.670+6787C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663510 | ||||||
| chr6:43663522
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+6799G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663522 | ||||||
| chr6:43663576
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670+6853G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663576 | ||||||
| chr6:43663592
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.670+6869G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663592 | ||||||
| chr6:43663643
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.670+6920T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663643 | ||||||
| chr6:43663659
|
C | T | 6 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0154others(3): Show | 6 | HG01346.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+6936C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663659 | ||||||
| chr6:43663737
|
AC | A | 6 | a0001c0001t0007g0254a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+7015delC | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663737 | ||||||
| chr6:43663757
|
C | T | 7 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-7032C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663757 | ||||||
| chr6:43663795
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.671-6994C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663795 | ||||||
| chr6:43663847
|
T | C | 46 | a0001c0001t0001g0129a0002c0002t0002g0002a0002c0002t0002g0007others(43): Show | 66 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.671-6942T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663847 | ||||||
| chr6:43663858
|
C | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(115): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.671-6931C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663858 | ||||||
| chr6:43663916
|
C | G | 3 | a0001c0001t0008g0006a0001c0001t0008g0100a0001c0001t0008g0101 | 6 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-6873C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663916 | ||||||
| chr6:43663936
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(63): Show | 80 | HG00642.hp2 HG01081.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.671-6853C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663936 | ||||||
| chr6:43663969
|
C | T | 7 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-6820C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43663969 | ||||||
| chr6:43664024
|
C | CT | 6 | a0001c0001t0007g0254a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6764dupT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43664024 | |||||
| chr6:43664026
|
C | A | 6 | a0001c0001t0007g0254a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 6 | HG02109.hp2 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6763C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | ||||||
| chr6:43664026
|
C | CA | 81 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(78): Show | 114 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.671-6763_671-6762i others(3): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | ||||||
| chr6:43664026
|
C | CAG | 7 | a0001c0001t0005g0032a0001c0001t0005g0079a0001c0001t0005g0080others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-6763_671-6762i others(4): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664026 | ||||||
| chr6:43664027
|
G | A | 30 | a0001c0001t0001g0117a0001c0001t0001g0239a0001c0001t0004g0066others(27): Show | 31 | HG00597.hp2 HG00639.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.671-6762G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664027 | ||||||
| chr6:43664028
|
A | G | 22 | a0001c0001t0001g0117a0001c0001t0001g0239a0001c0001t0004g0066others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.671-6761A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664028 | ||||||
| chr6:43664174
|
T | G | 1 | a0001c0001t0001g0015 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.671-6615T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664174 | ||||||
| chr6:43664177
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(114): Show | 151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.671-6612G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664177 | ||||||
| chr6:43664182
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.671-6607G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664182 | ||||||
| chr6:43664203
|
GTGATGA | G | 10 | a0001c0001t0003g0026a0001c0001t0003g0108a0001c0001t0003g0140others(7): Show | 12 | HG01257.hp2 HG01258.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.671-6566_671-6561d others(8): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43664203 | |||||
| chr6:43664220
|
G | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0100a0001c0001t0008g0101 | 6 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-6569G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664220 | ||||||
| chr6:43664223
|
G | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(28): Show | 43 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.671-6566G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664223 | ||||||
| chr6:43664226
|
G | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(62): Show | 78 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.671-6563G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664226 | ||||||
| chr6:43664322
|
C | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(18): Show | 30 | HG00642.hp2 HG01081.hp2 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.671-6467C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664322 | ||||||
| chr6:43664364
|
G | A | 45 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0009others(42): Show | 65 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.671-6425G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664364 | ||||||
| chr6:43664536
|
G | A | 1 | a0002c0002t0019g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-6253G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664536 | ||||||
| chr6:43664539
|
C | T | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-6250C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664539 | ||||||
| chr6:43664596
|
C | A | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-6193C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664596 | ||||||
| chr6:43664646
|
T | G | 6 | a0001c0001t0001g0117a0002c0002t0002g0085a0002c0002t0002g0086others(3): Show | 6 | HG00597.hp2 HG00639.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-6143T>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664646 | ||||||
| chr6:43664652
|
T | C | 52 | a0001c0001t0001g0117a0002c0002t0002g0002a0002c0002t0002g0007others(49): Show | 72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.671-6137T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664652 | ||||||
| chr6:43664711
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.671-6078G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664711 | ||||||
| chr6:43664748
|
G | C | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-6041G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664748 | ||||||
| chr6:43664874
|
G | A | 1 | a0001c0001t0009g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.671-5915G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664874 | ||||||
| chr6:43664950
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0175 | 2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.671-5839C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43664950 | ||||||
| chr6:43665205
|
G | C | 7 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-5584G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665205 | ||||||
| chr6:43665248
|
G | T | 1 | a0003c0003t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-5541G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665248 | ||||||
| chr6:43665305
|
G | A | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-5484G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665305 | ||||||
| chr6:43665365
|
A | G | 1 | a0001c0001t0004g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.671-5424A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665365 | ||||||
| chr6:43665466
|
T | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(116): Show | 152 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.671-5323T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665466 | ||||||
| chr6:43665483
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.671-5306A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665483 | ||||||
| chr6:43665558
|
G | A | 6 | a0001c0001t0009g0174a0001c0001t0009g0226a0001c0001t0009g0227others(3): Show | 7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-5231G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665558 | ||||||
| chr6:43665560
|
G | C | 7 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-5229G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665560 | ||||||
| chr6:43665710
|
A | T | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-5079A>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665710 | ||||||
| chr6:43665823
|
C | T | 57 | a0001c0001t0001g0105a0001c0001t0006g0037a0001c0001t0006g0073others(54): Show | 77 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.671-4966C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665823 | ||||||
| chr6:43665833
|
T | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0234a0001c0001t0001g0235 | 7 | HG02486.hp2 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-4956T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665833 | ||||||
| chr6:43665876
|
T | C | 4 | a0002c0002t0002g0113a0002c0002t0002g0155a0002c0002t0002g0211others(1): Show | 4 | HG00621.hp1 NA18945.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-4913T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665876 | ||||||
| chr6:43665980
|
C | A | 1 | a0002c0002t0002g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.671-4809C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665980 | ||||||
| chr6:43665983
|
G | A | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-4806G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43665983 | ||||||
| chr6:43666232
|
CT | C | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-4554delT | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43666232 | |||||
| chr6:43666448
|
A | G | 1 | a0002c0002t0002g0132 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.671-4341A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666448 | ||||||
| chr6:43666530
|
C | T | 5 | a0002c0002t0002g0085a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 5 | HG00639.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-4259C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666530 | ||||||
| chr6:43666637
|
C | T | 7 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(4): Show | 8 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-4152C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666637 | ||||||
| chr6:43666771
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.671-4018G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666771 | ||||||
| chr6:43666910
|
A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(19): Show | 31 | HG00597.hp2 HG00642.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.671-3879A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666910 | ||||||
| chr6:43666987
|
G | T | 7 | a0001c0001t0001g0105a0001c0001t0006g0073a0001c0001t0006g0207others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-3802G>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666987 | ||||||
| chr6:43666996
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.671-3793A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43666996 | ||||||
| chr6:43667005
|
A | C | 5 | a0001c0001t0003g0219a0001c0001t0003g0221a0001c0001t0011g0012others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-3784A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667005 | ||||||
| chr6:43667428
|
C | CCTGCCTG others(1): Show |
131 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(128): Show | 165 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.671-3355_671-3354i others(10): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43667428 | |||||
| chr6:43667494
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(32): Show | 47 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.671-3295G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667494 | ||||||
| chr6:43667514
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671-3275C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667514 | ||||||
| chr6:43667658
|
G | A | 11 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0074others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-3131G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667658 | ||||||
| chr6:43667681
|
C | CCCT | 53 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(50): Show | 74 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.671-3094_671-3092d others(5): Show |
RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43667681 | |||||
| chr6:43667737
|
C | T | 6 | a0001c0001t0009g0174a0001c0001t0009g0226a0001c0001t0009g0227others(3): Show | 7 | HG02451.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-3052C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667737 | ||||||
| chr6:43667864
|
T | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(32): Show | 47 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.671-2925T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43667864 | ||||||
| chr6:43668089
|
AG | A | 6 | a0001c0001t0006g0073a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-2695delG | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 43668089 | |||||
| chr6:43668120
|
A | C | 11 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0074others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-2669A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668120 | ||||||
| chr6:43668158
|
G | A | 1 | a0004c0004t0001g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.671-2631G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668158 | ||||||
| chr6:43668165
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.671-2624T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668165 | ||||||
| chr6:43668183
|
C | T | 1 | a0002c0002t0019g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-2606C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668183 | ||||||
| chr6:43668374
|
G | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(32): Show | 47 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.671-2415G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668374 | ||||||
| chr6:43668435
|
C | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671-2354C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668435 | ||||||
| chr6:43668435
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.671-2354C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668435 | ||||||
| chr6:43668441
|
C | T | 8 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(5): Show | 9 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-2348C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668441 | ||||||
| chr6:43668502
|
C | T | 1 | a0001c0001t0005g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-2287C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668502 | ||||||
| chr6:43668515
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.671-2274G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668515 | ||||||
| chr6:43668920
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.671-1869C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43668920 | ||||||
| chr6:43669047
|
A | C | 1 | a0001c0001t0005g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-1742A>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669047 | ||||||
| chr6:43669276
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.671-1513G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669276 | ||||||
| chr6:43669326
|
T | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(32): Show | 47 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.671-1463T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669326 | ||||||
| chr6:43669406
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0232a0001c0001t0001g0233 | 5 | NA18747.hp1 NA18974.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1383G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669406 | ||||||
| chr6:43669482
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.671-1307G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669482 | ||||||
| chr6:43669633
|
C | T | 1 | a0001c0001t0015g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-1156C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669633 | ||||||
| chr6:43669663
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.671-1126G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669663 | ||||||
| chr6:43669678
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0048others(7): Show | 12 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-1111G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669678 | ||||||
| chr6:43669862
|
A | G | 51 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0009others(48): Show | 71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.671-927A>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669862 | ||||||
| chr6:43669892
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0200 | 3 | NA18961.hp1 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.671-897G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669892 | ||||||
| chr6:43669906
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0146 | 3 | HG03831.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-883G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43669906 | ||||||
| chr6:43670024
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0145 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.671-765C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670024 | ||||||
| chr6:43670133
|
G | A | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-656G>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670133 | ||||||
| chr6:43670198
|
C | G | 1 | a0001c0001t0021g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.671-591C>G | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670198 | ||||||
| chr6:43670327
|
C | T | 1 | a0002c0002t0002g0121 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.671-462C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670327 | ||||||
| chr6:43670366
|
C | T | 1 | a0002c0002t0002g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.671-423C>T | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670366 | ||||||
| chr6:43670421
|
G | C | 1 | a0002c0002t0002g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.671-368G>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670421 | ||||||
| chr6:43670455
|
T | C | 17 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0147others(14): Show | 18 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.671-334T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670455 | ||||||
| chr6:43670667
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.671-122C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670667 | ||||||
| chr6:43670677
|
T | A | 1 | a0001c0001t0006g0246 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.671-112T>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670677 | ||||||
| chr6:43670685
|
T | C | 6 | a0001c0001t0006g0073a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG00741.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-104T>C | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670685 | ||||||
| chr6:43670748
|
C | A | 8 | a0001c0001t0005g0032a0001c0001t0005g0068a0001c0001t0005g0079others(5): Show | 9 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-41C>A | RSPH9 | ENSG00000172426.16 | transcript | ENST00000372163.5 | protein_coding | 4/4 | chr6 | 43670748 |