Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11172 |
|---|---|
| ensemblid | ENSG00000120210.8 |
| hgncid | 6089 |
| symbol | INSL6 |
| name | insulin like 6 |
| refseq_nuc | NM_007179.3 |
| refseq_prot | NP_009110.2 |
| ensembl_nuc | ENST00000381641.4 |
| ensembl_prot | ENSP00000371054.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 5163868 |
| end | 5185639 |
| strand | - |
| ver | v1.2 |
| region | chr9:5163868-5185639 |
| region5000 | chr9:5158868-5190639 |
| regionname0 | INSL6_chr9_5163868_5185639 |
| regionname5000 | INSL6_chr9_5158868_5190639 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 213 | 330 | 44 | 74 | 156 | 8 | 46 | 116 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002 | 0/0 | 213 | 38 | 36 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0003 | 0/0 | 213 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0004 | 0/0 | 213 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0005 | 0/0 | 213 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0006 | 0/0 | 213 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 642 | 324 | 41 | 71 | 156 | 8 | 46 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0002 | 0/0 | 642 | 36 | 34 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0003 | 0/0 | 642 | 9 | 8 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0004 | 0/0 | 642 | 3 | 0 | 3 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0005 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0006 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0007 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0008 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0009 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0010 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0011 | 0/0 | 642 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0012 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| c0013 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 83 | 379 | 90 | 78 | 156 | 8 | 45 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| t0002 | 0/0 | 83 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| t0003 | 0/0 | 83 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| t0004 | 0/0 | 83 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 61 | 1 | 13 | 40 | 1 | 6 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0002 | 0/0 | 24 | 0 | 3 | 18 | 0 | 3 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0003 | 0/0 | 13 | 2 | 4 | 3 | 3 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0004 | 0/1 | 12 | 0 | 9 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0006 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0010 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 642 | 324 | 41 | 71 | 156 | 8 | 46 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0004 | 0/0 | 642 | 3 | 0 | 3 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0009 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0012 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0013 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0002 | 0/0 | 642 | 36 | 34 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0008 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0010 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0003c0003 | 0/0 | 642 | 9 | 8 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0003c0007 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0004c0005 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0005c0006 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0006c0011 | 0/0 | 642 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 724 | 319 | 37 | 71 | 156 | 8 | 45 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0001t0002 | 0/0 | 724 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0001t0003 | 0/0 | 724 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0001t0004 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0004t0001 | 0/0 | 724 | 3 | 0 | 3 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0009t0001 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0012t0001 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0001c0013t0001 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0002t0001 | 0/0 | 724 | 36 | 34 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0008t0001 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0002c0010t0001 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0003c0003t0001 | 0/0 | 724 | 9 | 8 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0003c0007t0001 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0004c0005t0001 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0005c0006t0001 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| a0006c0011t0001 | 0/0 | 724 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | copy fasta | chr9 | 5158868 | 5190639 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 61 | 1 | 13 | 40 | 1 | 6 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0002 | 0/0 | 24 | 0 | 3 | 18 | 0 | 3 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0003 | 0/0 | 13 | 2 | 4 | 3 | 3 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0004 | 0/1 | 12 | 0 | 9 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0004t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0012t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0001c0013t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0002c0010t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0007t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0003c0007t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0004c0005t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0005c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| a0006c0011t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0045 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0180 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01993 | hp1 | a0006 | c0011 | t0001 | g0101 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0158 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02257 | hp2 | a0003 | c0007 | t0001 | g0176 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02572 | hp2 | a0002 | c0010 | t0001 | g0058 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0175 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0181 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0177 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0179 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03098 | hp2 | a0005 | c0006 | t0001 | g0030 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03139 | hp2 | a0001 | c0013 | t0001 | g0174 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03453 | hp2 | a0005 | c0006 | t0001 | g0030 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03486 | hp1 | a0003 | c0007 | t0001 | g0182 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ESN | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0178 | AFR | GWD | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ASW | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02109 | hp1 | a0002 | c0008 | t0001 | g0048 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02109 | hp2 | a0004 | c0005 | t0001 | g0027 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | USA | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA20300 | hp1 | a0001 | c0009 | t0001 | g0049 | AFR | USA | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA20300 | hp2 | a0001 | c0012 | t0001 | g0172 | AFR | USA | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | INSL6_chr9_5158868_5190639 | INSL6 | chr9 | 5158868 | 5190639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5164131
|
G | A | 1 | a0006 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.424C>T | p.His142Tyr | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 461/724 | 424/642 | 142/213 | chr9 | 5164131 | ||
| chr9:5164151
|
T | C | 1 | a0005 | 2 | HG03098.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.404A>G | p.His135Arg | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 441/724 | 404/642 | 135/213 | chr9 | 5164151 | ||
| chr9:5185365
|
A | G | 1 | a0002 | 38 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(35): Show |
missense_variant | MODERATE | c.238T>C | p.Phe80Leu | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 275/724 | 238/642 | 80/213 | chr9 | 5185365 | ||
| chr9:5185460
|
G | A | 1 | a0003 | 11 | HG01981.hp1 HG02257.hp2 HG02717.hp1 others(8): Show |
missense_variant | MODERATE | c.143C>T | p.Ala48Val | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 180/724 | 143/642 | 48/213 | chr9 | 5185460 | ||
| chr9:5185569
|
G | T | 1 | a0004 | 2 | HG02055.hp1 HG02109.hp2 |
missense_variant | MODERATE | c.34C>A | p.Leu12Ile | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 71/724 | 34/642 | 12/213 | chr9 | 5185569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5164096
|
G | A | 1 | a0001c0004 | 3 | HG01496.hp1 HG01943.hp2 HG02148.hp1 |
synonymous_variant | LOW | c.459C>T | p.Asn153Asn | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 496/724 | 459/642 | 153/213 | chr9 | 5164096 | ||
| chr9:5164138
|
T | G | 1 | a0002c0010 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.417A>C | p.Val139Val | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 454/724 | 417/642 | 139/213 | chr9 | 5164138 | ||
| chr9:5164144
|
G | A | 1 | a0001c0012 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.411C>T | p.Ile137Ile | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 448/724 | 411/642 | 137/213 | chr9 | 5164144 | ||
| chr9:5164183
|
G | A | 1 | a0003c0007 | 2 | HG02257.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.372C>T | p.Pro124Pro | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 409/724 | 372/642 | 124/213 | chr9 | 5164183 | ||
| chr9:5185381
|
G | C | 1 | a0001c0013 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.222C>G | p.Ala74Ala | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 259/724 | 222/642 | 74/213 | chr9 | 5185381 | ||
| chr9:5185540
|
A | T | 1 | a0001c0009 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.63T>A | p.Arg21Arg | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 100/724 | 63/642 | 21/213 | chr9 | 5185540 | ||
| chr9:5185597
|
C | T | 1 | a0002c0008 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.6G>A | p.Pro2Pro | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 43/724 | 6/642 | 2/213 | chr9 | 5185597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5163872
|
T | C | 1 | a0001c0001t0003 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 41 | chr9 | 5163872 | |||||
| chr9:5163897
|
A | G | 1 | a0001c0001t0002 | 3 | HG02055.hp2 HG02145.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 2/2 | 16 | chr9 | 5163897 | |||||
| chr9:5185609
|
G | C | 1 | a0001c0001t0004 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/2 | 7 | chr9 | 5185609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5164422
|
C | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0038others(4): Show | 10 | HG01074.hp2 HG01361.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-157G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164422 | ||||||
| chr9:5164477
|
G | A | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0003c0003t0001g0026others(7): Show | 12 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-212C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164477 | ||||||
| chr9:5164492
|
G | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(54): Show | 116 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.290-227C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164492 | ||||||
| chr9:5164551
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.290-286C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164551 | ||||||
| chr9:5164553
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.290-288T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164553 | ||||||
| chr9:5164596
|
C | G | 4 | a0001c0001t0001g0126a0003c0003t0001g0026a0003c0003t0001g0179others(1): Show | 6 | HG02717.hp1 HG02896.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-331G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164596 | ||||||
| chr9:5164659
|
C | T | 1 | a0001c0001t0001g0013 | 4 | NA18943.hp2 NA18961.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-394G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164659 | ||||||
| chr9:5164945
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.290-680G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164945 | ||||||
| chr9:5164964
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290-699G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164964 | ||||||
| chr9:5164992
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-727C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5164992 | ||||||
| chr9:5165067
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.290-802G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165067 | ||||||
| chr9:5165101
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.290-836G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165101 | ||||||
| chr9:5165136
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.290-871C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165136 | ||||||
| chr9:5165152
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0169 | 4 | NA18967.hp2 NA19009.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-887T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165152 | ||||||
| chr9:5165164
|
T | C | 2 | a0002c0002t0001g0053a0002c0002t0001g0059 | 2 | HG00639.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.290-899A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165164 | ||||||
| chr9:5165208
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.290-943G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165208 | ||||||
| chr9:5165210
|
C | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0165 | 3 | HG02055.hp2 HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.290-945G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165210 | ||||||
| chr9:5165230
|
T | C | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0003c0003t0001g0026others(7): Show | 12 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-965A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165230 | ||||||
| chr9:5165324
|
T | A | 1 | a0001c0001t0001g0019 | 3 | NA18939.hp2 NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.290-1059A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165324 | ||||||
| chr9:5165350
|
T | G | 1 | a0002c0002t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.290-1085A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165350 | ||||||
| chr9:5165408
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0050a0002c0008t0001g0048 | 5 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-1143C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165408 | ||||||
| chr9:5165427
|
C | T | 2 | a0004c0005t0001g0027a0005c0006t0001g0030 | 4 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-1162G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165427 | ||||||
| chr9:5165438
|
T | A | 1 | a0001c0001t0001g0039 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.290-1173A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165438 | ||||||
| chr9:5165439
|
T | G | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.290-1174A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165439 | ||||||
| chr9:5165542
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.290-1277T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165542 | ||||||
| chr9:5165573
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-1308A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165573 | ||||||
| chr9:5165587
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.290-1322G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165587 | ||||||
| chr9:5165619
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.290-1354A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165619 | ||||||
| chr9:5165683
|
T | C | 3 | a0001c0009t0001g0049a0004c0005t0001g0027a0005c0006t0001g0030 | 5 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-1418A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165683 | ||||||
| chr9:5165703
|
C | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0170 | 5 | NA18967.hp2 NA19009.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-1438G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165703 | ||||||
| chr9:5165818
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290-1553G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165818 | ||||||
| chr9:5165861
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-1596A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165861 | ||||||
| chr9:5165925
|
C | A | 6 | a0002c0002t0001g0016a0002c0002t0001g0028a0002c0002t0001g0050others(3): Show | 9 | HG01884.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.290-1660G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165925 | ||||||
| chr9:5165980
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.290-1715G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5165980 | ||||||
| chr9:5166179
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.290-1914G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166179 | ||||||
| chr9:5166197
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.290-1932C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166197 | ||||||
| chr9:5166273
|
G | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(42): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.290-2008C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166273 | ||||||
| chr9:5166295
|
GT | G | 3 | a0001c0001t0001g0160a0001c0004t0001g0045a0001c0004t0001g0158 | 4 | HG01496.hp1 HG01943.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2031delA | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166295 | ||||||
| chr9:5166314
|
T | TCC | 5 | a0001c0001t0001g0014a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 8 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-2051_290-2050d others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166314 | ||||||
| chr9:5166315
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0146 | 4 | NA18986.hp2 NA19000.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2050G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166315 | ||||||
| chr9:5166466
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.290-2201T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166466 | ||||||
| chr9:5166548
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(79): Show | 162 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.290-2283G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166548 | ||||||
| chr9:5166642
|
A | T | 1 | a0002c0002t0001g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2377T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166642 | ||||||
| chr9:5166682
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.290-2417G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166682 | ||||||
| chr9:5166840
|
G | C | 5 | a0002c0002t0001g0008a0002c0002t0001g0051a0002c0002t0001g0052others(2): Show | 10 | HG02257.hp1 HG02559.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-2575C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166840 | ||||||
| chr9:5166942
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0170 | 5 | NA18967.hp2 NA19009.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-2677C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166942 | ||||||
| chr9:5166966
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-2701C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5166966 | ||||||
| chr9:5167035
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.290-2770C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167035 | ||||||
| chr9:5167196
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0050a0002c0008t0001g0048 | 5 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-2931C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167196 | ||||||
| chr9:5167245
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.290-2980G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167245 | ||||||
| chr9:5167272
|
T | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0136others(5): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.290-3007A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167272 | ||||||
| chr9:5167314
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.290-3049T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167314 | ||||||
| chr9:5167342
|
G | T | 1 | a0001c0001t0002g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290-3077C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167342 | ||||||
| chr9:5167487
|
G | A | 1 | a0001c0001t0001g0025 | 3 | NA18967.hp2 NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.290-3222C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167487 | ||||||
| chr9:5167510
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.290-3245G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167510 | ||||||
| chr9:5167611
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 6 | NA18612.hp2 NA18967.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-3346C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167611 | ||||||
| chr9:5167649
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(98): Show | 185 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.290-3384T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167649 | ||||||
| chr9:5167650
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.290-3385G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167650 | ||||||
| chr9:5167712
|
G | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(80): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.290-3447C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167712 | ||||||
| chr9:5167788
|
A | C | 3 | a0002c0002t0001g0016a0002c0002t0001g0050a0002c0008t0001g0048 | 5 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-3523T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167788 | ||||||
| chr9:5167808
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0065others(24): Show | 46 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.290-3543G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167808 | ||||||
| chr9:5167824
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.290-3559C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167824 | ||||||
| chr9:5167838
|
C | A | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0065others(24): Show | 46 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.290-3573G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167838 | ||||||
| chr9:5167912
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.290-3647G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167912 | ||||||
| chr9:5167918
|
G | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0065others(27): Show | 51 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.290-3653C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167918 | ||||||
| chr9:5167921
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 383 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.290-3656A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5167921 | ||||||
| chr9:5168013
|
A | C | 31 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0065others(28): Show | 52 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.290-3748T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168013 | ||||||
| chr9:5168137
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(56): Show | 121 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.290-3872G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168137 | ||||||
| chr9:5168141
|
G | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG02135.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.290-3876C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168141 | ||||||
| chr9:5168199
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(5): Show | 13 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.290-3934C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168199 | ||||||
| chr9:5168313
|
A | C | 2 | a0001c0009t0001g0049a0004c0005t0001g0027 | 3 | HG02055.hp1 HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.290-4048T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168313 | ||||||
| chr9:5168346
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.290-4081A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168346 | ||||||
| chr9:5168389
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.290-4124C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168389 | ||||||
| chr9:5168585
|
C | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 376 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.290-4320G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168585 | ||||||
| chr9:5168612
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.290-4347G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168612 | ||||||
| chr9:5168682
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.290-4417G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168682 | ||||||
| chr9:5168690
|
TAGCA | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(6): Show | 14 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-4429_290-4426d others(6): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168690 | ||||||
| chr9:5168778
|
C | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-4513G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168778 | ||||||
| chr9:5168805
|
G | GAAAA | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(97): Show | 184 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.290-4541_290-4540i others(6): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168805 | ||||||
| chr9:5168871
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(41): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.290-4606C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168871 | ||||||
| chr9:5168907
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.290-4642C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168907 | ||||||
| chr9:5168927
|
AT | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(83): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.290-4663delA | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168927 | ||||||
| chr9:5168927
|
ATT | A | 15 | a0001c0001t0001g0065a0001c0001t0001g0126a0001c0001t0001g0127others(12): Show | 17 | HG00741.hp2 HG01981.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.290-4664_290-4663d others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168927 | ||||||
| chr9:5168962
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-4697C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168962 | ||||||
| chr9:5168967
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.290-4702G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168967 | ||||||
| chr9:5168994
|
C | G | 3 | a0001c0009t0001g0049a0004c0005t0001g0027a0005c0006t0001g0030 | 5 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-4729G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168994 | ||||||
| chr9:5168995
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(41): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.290-4730C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5168995 | ||||||
| chr9:5169087
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(5): Show | 13 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.290-4822G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169087 | ||||||
| chr9:5169302
|
G | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(76): Show | 159 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.290-5037C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169302 | ||||||
| chr9:5169433
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290-5168G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169433 | ||||||
| chr9:5169715
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-5450C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169715 | ||||||
| chr9:5169751
|
A | G | 1 | a0001c0001t0001g0017 | 3 | HG01358.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.290-5486T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169751 | ||||||
| chr9:5169804
|
A | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(41): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.290-5539T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169804 | ||||||
| chr9:5169814
|
T | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(81): Show | 165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.290-5549A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169814 | ||||||
| chr9:5169885
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.290-5620C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169885 | ||||||
| chr9:5169910
|
T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG00741.hp2 HG02723.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-5645A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169910 | ||||||
| chr9:5169913
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.290-5648A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169913 | ||||||
| chr9:5169915
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.290-5650C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169915 | ||||||
| chr9:5169916
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.290-5651A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169916 | ||||||
| chr9:5169931
|
C | T | 1 | a0003c0003t0001g0178 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.290-5666G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169931 | ||||||
| chr9:5169951
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG01433.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.290-5686A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169951 | ||||||
| chr9:5169975
|
A | G | 14 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(11): Show | 16 | HG00741.hp2 HG01981.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.290-5710T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5169975 | ||||||
| chr9:5170080
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(98): Show | 185 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.290-5815C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170080 | ||||||
| chr9:5170212
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290-5947T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170212 | ||||||
| chr9:5170220
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.290-5955T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170220 | ||||||
| chr9:5170399
|
T | C | 1 | a0004c0005t0001g0027 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.290-6134A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170399 | ||||||
| chr9:5170440
|
T | C | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-6175A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170440 | ||||||
| chr9:5170528
|
C | G | 1 | a0001c0001t0001g0036 | 2 | HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.290-6263G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170528 | ||||||
| chr9:5170546
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.290-6281T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170546 | ||||||
| chr9:5170556
|
C | CT | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(80): Show | 160 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.290-6292dupA | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170556 | ||||||
| chr9:5170600
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290-6335C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170600 | ||||||
| chr9:5170645
|
G | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(98): Show | 185 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.290-6380C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170645 | ||||||
| chr9:5170797
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.290-6532A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5170797 | ||||||
| chr9:5171057
|
T | G | 1 | a0001c0001t0001g0023 | 3 | NA18986.hp2 NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.290-6792A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171057 | ||||||
| chr9:5171082
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.290-6817G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171082 | ||||||
| chr9:5171236
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.290-6971G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171236 | ||||||
| chr9:5171333
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.290-7068A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171333 | ||||||
| chr9:5171350
|
C | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-7085G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171350 | ||||||
| chr9:5171526
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0170 | 5 | NA18967.hp2 NA19009.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-7261C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171526 | ||||||
| chr9:5171701
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.290-7436C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171701 | ||||||
| chr9:5171745
|
C | G | 1 | a0001c0001t0001g0032 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.290-7480G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171745 | ||||||
| chr9:5171889
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-7624G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171889 | ||||||
| chr9:5171944
|
T | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(101): Show | 188 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.290-7679A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171944 | ||||||
| chr9:5171992
|
G | C | 1 | a0001c0012t0001g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290-7727C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171992 | ||||||
| chr9:5171995
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.290-7730C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5171995 | ||||||
| chr9:5172027
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290-7762G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172027 | ||||||
| chr9:5172183
|
C | T | 11 | a0001c0001t0001g0065a0002c0002t0001g0005a0002c0002t0001g0029others(8): Show | 20 | HG00639.hp2 HG00741.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-7918G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172183 | ||||||
| chr9:5172188
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.290-7923T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172188 | ||||||
| chr9:5172375
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.290-8110T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172375 | ||||||
| chr9:5172389
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290-8124G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172389 | ||||||
| chr9:5172397
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-8132A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172397 | ||||||
| chr9:5172540
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(74): Show | 151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.290-8275C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172540 | ||||||
| chr9:5172567
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(77): Show | 155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.290-8302C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172567 | ||||||
| chr9:5172631
|
G | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-8366C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172631 | ||||||
| chr9:5172770
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290-8505C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172770 | ||||||
| chr9:5172789
|
G | A | 1 | a0002c0002t0001g0029 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.290-8524C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172789 | ||||||
| chr9:5172841
|
T | C | 1 | a0002c0008t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-8576A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172841 | ||||||
| chr9:5172907
|
G | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(44): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.290-8642C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172907 | ||||||
| chr9:5172991
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-8726A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5172991 | ||||||
| chr9:5173088
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290-8823T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173088 | ||||||
| chr9:5173107
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | NA18942.hp1 NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.290-8842A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173107 | ||||||
| chr9:5173120
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0067 | 6 | HG01081.hp1 HG01255.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-8855C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173120 | ||||||
| chr9:5173161
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.290-8896A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173161 | ||||||
| chr9:5173205
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(7): Show | 16 | HG01192.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-8940C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173205 | ||||||
| chr9:5173227
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.290-8962C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173227 | ||||||
| chr9:5173319
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.290-9054A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173319 | ||||||
| chr9:5173399
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(81): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.290-9134G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173399 | ||||||
| chr9:5173406
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.290-9141T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173406 | ||||||
| chr9:5173481
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-9216G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173481 | ||||||
| chr9:5173498
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.290-9233G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173498 | ||||||
| chr9:5173540
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-9275T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173540 | ||||||
| chr9:5173592
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.290-9327G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173592 | ||||||
| chr9:5173594
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.290-9329G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173594 | ||||||
| chr9:5173776
|
T | TA | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0086others(3): Show | 10 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-9512dupT | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173776 | ||||||
| chr9:5173776
|
TA | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(47): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.290-9512delT | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173776 | ||||||
| chr9:5173816
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290-9551G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173816 | ||||||
| chr9:5173868
|
G | C | 11 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0139others(8): Show | 13 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.290-9603C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5173868 | ||||||
| chr9:5174035
|
C | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-9770G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174035 | ||||||
| chr9:5174221
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290-9956G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174221 | ||||||
| chr9:5174253
|
A | C | 2 | a0003c0007t0001g0176a0003c0007t0001g0182 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.290-9988T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174253 | ||||||
| chr9:5174268
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.290-10003A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174268 | ||||||
| chr9:5174284
|
T | A | 1 | a0001c0012t0001g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290-10019A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174284 | ||||||
| chr9:5174372
|
A | C | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-10107T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174372 | ||||||
| chr9:5174590
|
T | G | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.290-10325A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174590 | ||||||
| chr9:5174638
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(82): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.290-10373A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174638 | ||||||
| chr9:5174673
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(5): Show | 13 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.290-10408G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174673 | ||||||
| chr9:5174754
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.290-10489G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174754 | ||||||
| chr9:5174771
|
C | A | 2 | a0002c0002t0001g0016a0002c0002t0001g0050 | 4 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-10506G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174771 | ||||||
| chr9:5174782
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.290-10517G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174782 | ||||||
| chr9:5174800
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.289+10514G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174800 | ||||||
| chr9:5174829
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(82): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.289+10485G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174829 | ||||||
| chr9:5174939
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.289+10375T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174939 | ||||||
| chr9:5174940
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.289+10374A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174940 | ||||||
| chr9:5174942
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.289+10372G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174942 | ||||||
| chr9:5174942
|
CT | C | 14 | a0001c0001t0001g0075a0002c0002t0001g0005a0002c0002t0001g0028others(11): Show | 24 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.289+10371delA | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174942 | ||||||
| chr9:5174970
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.289+10344G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174970 | ||||||
| chr9:5174996
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.289+10318C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5174996 | ||||||
| chr9:5175058
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+10256C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175058 | ||||||
| chr9:5175059
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 240 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.289+10255A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175059 | ||||||
| chr9:5175074
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(42): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.289+10240C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175074 | ||||||
| chr9:5175165
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.289+10149G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175165 | ||||||
| chr9:5175288
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(82): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.289+10026G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175288 | ||||||
| chr9:5175523
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(5): Show | 13 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+9791C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175523 | ||||||
| chr9:5175608
|
G | C | 1 | a0001c0001t0001g0024 | 3 | NA18971.hp2 NA19058.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.289+9706C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175608 | ||||||
| chr9:5175621
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(44): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.289+9693A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175621 | ||||||
| chr9:5175650
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.289+9664C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175650 | ||||||
| chr9:5175681
|
A | G | 5 | a0001c0001t0001g0126a0001c0009t0001g0049a0002c0002t0001g0016others(2): Show | 7 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+9633T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175681 | ||||||
| chr9:5175687
|
G | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(44): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.289+9627C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175687 | ||||||
| chr9:5175697
|
G | C | 19 | a0001c0001t0001g0065a0002c0002t0001g0005a0002c0002t0001g0008others(16): Show | 34 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.289+9617C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175697 | ||||||
| chr9:5175879
|
T | C | 18 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0028others(15): Show | 33 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.289+9435A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175879 | ||||||
| chr9:5175938
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(42): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.289+9376G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5175938 | ||||||
| chr9:5176147
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(82): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.289+9167G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176147 | ||||||
| chr9:5176215
|
C | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(83): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.289+9099G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176215 | ||||||
| chr9:5176281
|
C | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(64): Show | 130 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.289+9033G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176281 | ||||||
| chr9:5176352
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(83): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.289+8962G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176352 | ||||||
| chr9:5176374
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.289+8940G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176374 | ||||||
| chr9:5176388
|
A | G | 1 | a0001c0004t0001g0158 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.289+8926T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176388 | ||||||
| chr9:5176447
|
T | C | 1 | a0004c0005t0001g0027 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.289+8867A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176447 | ||||||
| chr9:5176454
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.289+8860T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176454 | ||||||
| chr9:5176681
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.289+8633C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176681 | ||||||
| chr9:5176683
|
G | A | 1 | a0002c0002t0001g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.289+8631C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176683 | ||||||
| chr9:5176698
|
G | A | 1 | a0001c0001t0001g0043 | 2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.289+8616C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176698 | ||||||
| chr9:5176719
|
CA | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0035others(14): Show | 31 | HG00597.hp2 HG01074.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.289+8594delT | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176719 | ||||||
| chr9:5176719
|
CAA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(87): Show | 166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.289+8593_289+8594d others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176719 | ||||||
| chr9:5176733
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.289+8581T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5176733 | ||||||
| chr9:5177027
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.289+8287G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177027 | ||||||
| chr9:5177072
|
G | C | 2 | a0004c0005t0001g0027a0005c0006t0001g0030 | 4 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+8242C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177072 | ||||||
| chr9:5177095
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.289+8219T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177095 | ||||||
| chr9:5177129
|
G | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+8185C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177129 | ||||||
| chr9:5177198
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+8116G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177198 | ||||||
| chr9:5177203
|
T | C | 1 | a0002c0008t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.289+8111A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177203 | ||||||
| chr9:5177331
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.289+7983G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177331 | ||||||
| chr9:5177338
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0132others(5): Show | 13 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+7976G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177338 | ||||||
| chr9:5177353
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.289+7961G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177353 | ||||||
| chr9:5177462
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 167 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.289+7852G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177462 | ||||||
| chr9:5177484
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.289+7830G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177484 | ||||||
| chr9:5177533
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 167 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.289+7781A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177533 | ||||||
| chr9:5177572
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.289+7742C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177572 | ||||||
| chr9:5177573
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 167 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.289+7741A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177573 | ||||||
| chr9:5177666
|
T | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 6 | NA18612.hp2 NA18967.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+7648A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177666 | ||||||
| chr9:5177680
|
C | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(88): Show | 171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.289+7634G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177680 | ||||||
| chr9:5177685
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 167 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.289+7629T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177685 | ||||||
| chr9:5177767
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.289+7547G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177767 | ||||||
| chr9:5177775
|
G | T | 15 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0029others(12): Show | 29 | HG00639.hp2 HG00741.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.289+7539C>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177775 | ||||||
| chr9:5177838
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.289+7476G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177838 | ||||||
| chr9:5177872
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(91): Show | 175 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.289+7442G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177872 | ||||||
| chr9:5177937
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(88): Show | 171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.289+7377C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177937 | ||||||
| chr9:5177987
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.289+7327G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177987 | ||||||
| chr9:5177988
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.289+7326C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177988 | ||||||
| chr9:5177995
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.289+7319G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5177995 | ||||||
| chr9:5178001
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(89): Show | 173 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.289+7313T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178001 | ||||||
| chr9:5178023
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.289+7291T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178023 | ||||||
| chr9:5178033
|
G | A | 1 | a0001c0001t0001g0018 | 3 | HG00642.hp1 HG01978.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.289+7281C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178033 | ||||||
| chr9:5178192
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.289+7122G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178192 | ||||||
| chr9:5178215
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.289+7099C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178215 | ||||||
| chr9:5178298
|
C | T | 18 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0028others(15): Show | 33 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.289+7016G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178298 | ||||||
| chr9:5178347
|
T | C | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+6967A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178347 | ||||||
| chr9:5178391
|
G | A | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+6923C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178391 | ||||||
| chr9:5178404
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.289+6910C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178404 | ||||||
| chr9:5178432
|
A | G | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+6882T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178432 | ||||||
| chr9:5178447
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.289+6867G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178447 | ||||||
| chr9:5178452
|
C | T | 1 | a0001c0001t0001g0034 | 2 | NA18960.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.289+6862G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178452 | ||||||
| chr9:5178482
|
G | A | 2 | a0001c0001t0001g0154a0001c0009t0001g0049 | 2 | HG00609.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.289+6832C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178482 | ||||||
| chr9:5178554
|
G | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+6760C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178554 | ||||||
| chr9:5178579
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(86): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+6735G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178579 | ||||||
| chr9:5178604
|
A | T | 1 | a0002c0002t0001g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.289+6710T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178604 | ||||||
| chr9:5178638
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.289+6676A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178638 | ||||||
| chr9:5178665
|
G | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+6649C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178665 | ||||||
| chr9:5178713
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.289+6601G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178713 | ||||||
| chr9:5178883
|
T | C | 9 | a0001c0001t0001g0127a0003c0003t0001g0026a0003c0003t0001g0177others(6): Show | 11 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+6431A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178883 | ||||||
| chr9:5178933
|
T | C | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+6381A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178933 | ||||||
| chr9:5178945
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.289+6369C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5178945 | ||||||
| chr9:5179002
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(86): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+6312G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179002 | ||||||
| chr9:5179010
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.289+6304G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179010 | ||||||
| chr9:5179044
|
C | CA | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0039others(40): Show | 76 | HG00639.hp2 HG00741.hp1 HG01258.hp1 others(73): Show |
intron_variant | MODIFIER | c.289+6269dupT | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179044 | ||||||
| chr9:5179044
|
C | CAA | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(53): Show | 114 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.289+6268_289+6269d others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179044 | ||||||
| chr9:5179195
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.289+6119C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179195 | ||||||
| chr9:5179332
|
G | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+5982C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179332 | ||||||
| chr9:5179423
|
G | A | 1 | a0002c0002t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+5891C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179423 | ||||||
| chr9:5179459
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.289+5855G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179459 | ||||||
| chr9:5179494
|
G | GTA | 19 | a0001c0001t0001g0065a0002c0002t0001g0005a0002c0002t0001g0008others(16): Show | 34 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.289+5819_289+5820i others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179494 | ||||||
| chr9:5179522
|
C | A | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+5792G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179522 | ||||||
| chr9:5179554
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.289+5760A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179554 | ||||||
| chr9:5179664
|
A | G | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+5650T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179664 | ||||||
| chr9:5179683
|
T | C | 1 | a0001c0001t0002g0046 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.289+5631A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179683 | ||||||
| chr9:5179702
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+5612C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179702 | ||||||
| chr9:5179745
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.289+5569G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179745 | ||||||
| chr9:5179758
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.289+5556G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179758 | ||||||
| chr9:5179865
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(88): Show | 171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.289+5449T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179865 | ||||||
| chr9:5179868
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.289+5446A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179868 | ||||||
| chr9:5179880
|
T | C | 1 | a0001c0001t0001g0043 | 2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.289+5434A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179880 | ||||||
| chr9:5179920
|
G | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(42): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.289+5394C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179920 | ||||||
| chr9:5179980
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.289+5334G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5179980 | ||||||
| chr9:5180039
|
T | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0156 | 4 | HG02735.hp1 HG02738.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+5275A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180039 | ||||||
| chr9:5180065
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0157a0001c0001t0001g0159others(3): Show | 18 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.289+5249A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180065 | ||||||
| chr9:5180068
|
G | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(41): Show | 96 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.289+5246C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180068 | ||||||
| chr9:5180080
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0128 | 2 | HG03225.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.289+5234C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180080 | ||||||
| chr9:5180144
|
A | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0033 | 5 | HG00642.hp1 HG00642.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+5170T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180144 | ||||||
| chr9:5180242
|
G | C | 3 | a0002c0002t0001g0028a0002c0002t0001g0063a0002c0002t0001g0064 | 4 | HG01884.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+5072C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180242 | ||||||
| chr9:5180287
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289+5027G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180287 | ||||||
| chr9:5180294
|
T | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0050 | 4 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+5020A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180294 | ||||||
| chr9:5180300
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.289+5014T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180300 | ||||||
| chr9:5180315
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 129 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.289+4999G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180315 | ||||||
| chr9:5180370
|
G | A | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+4944C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180370 | ||||||
| chr9:5180372
|
A | C | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+4942T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180372 | ||||||
| chr9:5180377
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.289+4937G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180377 | ||||||
| chr9:5180378
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289+4936A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180378 | ||||||
| chr9:5180393
|
T | C | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+4921A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180393 | ||||||
| chr9:5180546
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+4768C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180546 | ||||||
| chr9:5180547
|
C | A | 1 | a0001c0001t0001g0041 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.289+4767G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180547 | ||||||
| chr9:5180548
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(53): Show | 113 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.289+4766G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180548 | ||||||
| chr9:5180604
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(17): Show | 43 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.289+4710G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180604 | ||||||
| chr9:5180672
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.289+4642C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180672 | ||||||
| chr9:5180680
|
G | C | 9 | a0001c0001t0001g0127a0003c0003t0001g0026a0003c0003t0001g0177others(6): Show | 11 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+4634C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180680 | ||||||
| chr9:5180718
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.289+4596G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180718 | ||||||
| chr9:5180793
|
T | C | 4 | a0001c0001t0001g0126a0002c0002t0001g0016a0002c0002t0001g0050others(1): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+4521A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180793 | ||||||
| chr9:5180874
|
T | C | 1 | a0004c0005t0001g0027 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.289+4440A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180874 | ||||||
| chr9:5180887
|
T | G | 2 | a0001c0001t0001g0073a0001c0009t0001g0049 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.289+4427A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180887 | ||||||
| chr9:5180933
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0165 | 3 | HG02055.hp2 HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.289+4381G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180933 | ||||||
| chr9:5180961
|
A | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(87): Show | 170 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.289+4353T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180961 | ||||||
| chr9:5180996
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(100): Show | 186 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.289+4318A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5180996 | ||||||
| chr9:5181003
|
T | C | 19 | a0001c0001t0001g0065a0002c0002t0001g0005a0002c0002t0001g0008others(16): Show | 34 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.289+4311A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181003 | ||||||
| chr9:5181061
|
A | T | 1 | a0001c0001t0001g0032 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.289+4253T>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181061 | ||||||
| chr9:5181095
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.289+4219A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181095 | ||||||
| chr9:5181110
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.289+4204G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181110 | ||||||
| chr9:5181135
|
C | T | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+4179G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181135 | ||||||
| chr9:5181301
|
C | A | 2 | a0002c0002t0001g0016a0002c0002t0001g0050 | 4 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+4013G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181301 | ||||||
| chr9:5181319
|
C | T | 2 | a0001c0001t0002g0046a0002c0002t0001g0051 | 3 | HG02055.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.289+3995G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181319 | ||||||
| chr9:5181342
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289+3972G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181342 | ||||||
| chr9:5181424
|
G | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0165 | 3 | HG02055.hp2 HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.289+3890C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181424 | ||||||
| chr9:5181467
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(99): Show | 185 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.289+3847G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181467 | ||||||
| chr9:5181610
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(86): Show | 169 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.289+3704A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181610 | ||||||
| chr9:5181875
|
A | G | 1 | a0001c0012t0001g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.289+3439T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181875 | ||||||
| chr9:5181917
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.289+3397G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181917 | ||||||
| chr9:5181922
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.289+3392A>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181922 | ||||||
| chr9:5181952
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.289+3362G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5181952 | ||||||
| chr9:5182029
|
A | G | 2 | a0001c0001t0001g0073a0001c0009t0001g0049 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.289+3285T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182029 | ||||||
| chr9:5182159
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+3155G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182159 | ||||||
| chr9:5182301
|
TA | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+3012delT | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182301 | ||||||
| chr9:5182316
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 6 | NA18612.hp2 NA18967.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+2998C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182316 | ||||||
| chr9:5182337
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.289+2977T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182337 | ||||||
| chr9:5182430
|
G | C | 1 | a0001c0009t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.289+2884C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182430 | ||||||
| chr9:5182468
|
A | C | 1 | a0001c0001t0001g0031 | 2 | HG01981.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.289+2846T>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182468 | ||||||
| chr9:5182516
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.289+2798T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182516 | ||||||
| chr9:5182537
|
A | G | 19 | a0001c0001t0001g0065a0002c0002t0001g0005a0002c0002t0001g0008others(16): Show | 34 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.289+2777T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182537 | ||||||
| chr9:5182582
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0116others(5): Show | 17 | HG02056.hp1 HG03834.hp1 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+2732A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182582 | ||||||
| chr9:5182587
|
C | G | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0003c0003t0001g0026others(7): Show | 12 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+2727G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182587 | ||||||
| chr9:5182604
|
G | C | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0003c0003t0001g0026others(7): Show | 12 | HG01981.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+2710C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182604 | ||||||
| chr9:5182630
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.289+2684T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182630 | ||||||
| chr9:5182781
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.289+2533C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182781 | ||||||
| chr9:5182823
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.289+2491G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182823 | ||||||
| chr9:5182831
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0123 | 3 | HG01070.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.289+2483A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182831 | ||||||
| chr9:5182842
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0050a0002c0008t0001g0048 | 5 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+2472C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182842 | ||||||
| chr9:5182960
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+2354T>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182960 | ||||||
| chr9:5182992
|
T | C | 2 | a0001c0009t0001g0049a0004c0005t0001g0027 | 3 | HG02055.hp1 HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.289+2322A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5182992 | ||||||
| chr9:5183028
|
T | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(85): Show | 168 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.289+2286A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183028 | ||||||
| chr9:5183146
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.289+2168A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183146 | ||||||
| chr9:5183214
|
T | C | 3 | a0002c0002t0001g0028a0002c0002t0001g0063a0002c0002t0001g0064 | 4 | HG01884.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+2100A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183214 | ||||||
| chr9:5183463
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.289+1851A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183463 | ||||||
| chr9:5183639
|
T | G | 1 | a0002c0002t0001g0029 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.289+1675A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183639 | ||||||
| chr9:5183774
|
G | A | 1 | a0001c0012t0001g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.289+1540C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183774 | ||||||
| chr9:5183774
|
GAA | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 6 | HG02622.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+1538_289+1539d others(4): Show |
INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183774 | ||||||
| chr9:5183789
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.289+1525C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183789 | ||||||
| chr9:5183892
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(87): Show | 170 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.289+1422A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183892 | ||||||
| chr9:5183995
|
G | A | 21 | a0002c0002t0001g0005a0002c0002t0001g0008a0002c0002t0001g0016others(18): Show | 38 | HG00639.hp2 HG00741.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.289+1319C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5183995 | ||||||
| chr9:5184013
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.289+1301A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184013 | ||||||
| chr9:5184024
|
C | A | 2 | a0001c0009t0001g0049a0005c0006t0001g0030 | 3 | HG03098.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.289+1290G>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184024 | ||||||
| chr9:5184157
|
C | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00741.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+1157G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184157 | ||||||
| chr9:5184183
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.289+1131A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184183 | ||||||
| chr9:5184208
|
C | T | 1 | a0005c0006t0001g0030 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289+1106G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184208 | ||||||
| chr9:5184222
|
T | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 128 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.289+1092A>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184222 | ||||||
| chr9:5184313
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0050a0002c0008t0001g0048 | 5 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+1001C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184313 | ||||||
| chr9:5184425
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.289+889A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184425 | ||||||
| chr9:5184449
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(80): Show | 159 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.289+865C>T | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184449 | ||||||
| chr9:5184634
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.289+680G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184634 | ||||||
| chr9:5184787
|
T | C | 1 | a0001c0001t0001g0047 | 2 | NA18956.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.289+527A>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184787 | ||||||
| chr9:5184838
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.289+476G>A | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5184838 | ||||||
| chr9:5185124
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.289+190G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5185124 | ||||||
| chr9:5185151
|
G | C | 1 | a0004c0005t0001g0027 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.289+163C>G | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5185151 | ||||||
| chr9:5185290
|
C | G | 1 | a0002c0008t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.289+24G>C | INSL6 | ENSG00000120210.8 | transcript | ENST00000381641.4 | protein_coding | 1/1 | chr9 | 5185290 |