| geneid | 196740 |
|---|---|
| ensemblid | ENSG00000165633.13 |
| hgncid | 26470 |
| symbol | VSTM4 |
| name | V-set and transmembrane domain containing 4 |
| refseq_nuc | NM_001031746.5 |
| refseq_prot | NP_001026916.2 |
| ensembl_nuc | ENST00000332853.9 |
| ensembl_prot | ENSP00000331062.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 49014236 |
| end | 49115522 |
| strand | - |
| ver | v1.2 |
| region | chr10:49014236-49115522 |
| region5000 | chr10:49009236-49120522 |
| regionname0 | VSTM4_chr10_49014236_49115522 |
| regionname5000 | VSTM4_chr10_49009236_49120522 |
| 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 | 0/1 | 320 | 154 | 60 | 33 | 39 | 7 | 14 | 30 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002 | 1/0 | 320 | 121 | 23 | 19 | 59 | 3 | 16 | 42 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0003 | 0/0 | 320 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0004 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0005 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0006 | 0/0 | 320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| 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 | 0/1 | 963 | 126 | 39 | 29 | 37 | 7 | 13 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0002 | 0/0 | 963 | 120 | 23 | 19 | 59 | 3 | 16 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0003 | 0/0 | 963 | 19 | 16 | 3 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0004 | 0/0 | 963 | 4 | 1 | 0 | 2 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0005 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0006 | 0/0 | 963 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0007 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0008 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0009 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0010 | 1/0 | 963 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| c0011 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| 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 | 0/0 | 5445 | 67 | 12 | 12 | 33 | 4 | 6 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0002 | 0/0 | 5440 | 37 | 3 | 10 | 16 | 1 | 7 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0003 | 0/0 | 5447 | 27 | 12 | 0 | 13 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0004 | 1/0 | 5452 | 18 | 15 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0005 | 0/0 | 5448 | 14 | 0 | 0 | 14 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0006 | 0/0 | 5444 | 12 | 4 | 2 | 1 | 1 | 4 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0007 | 0/0 | 5440 | 11 | 1 | 1 | 3 | 1 | 5 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0008 | 0/1 | 5444 | 10 | 0 | 5 | 0 | 2 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0009 | 0/0 | 5439 | 8 | 8 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0010 | 0/0 | 5440 | 6 | 0 | 0 | 6 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0011 | 0/0 | 5443 | 5 | 5 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0012 | 0/0 | 5445 | 4 | 0 | 2 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0013 | 0/0 | 5444 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0014 | 0/0 | 5446 | 4 | 0 | 0 | 3 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0015 | 0/0 | 5443 | 3 | 2 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0016 | 0/0 | 5444 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0017 | 0/0 | 5441 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0018 | 0/0 | 5448 | 3 | 1 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0019 | 0/0 | 5448 | 3 | 0 | 1 | 0 | 1 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0020 | 0/0 | 5446 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0021 | 0/0 | 5448 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0022 | 0/0 | 5440 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0023 | 0/0 | 5440 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0024 | 0/0 | 5443 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0025 | 0/0 | 5448 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0026 | 0/0 | 5444 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0027 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0028 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0029 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0030 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0031 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0032 | 0/0 | 5445 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0033 | 0/0 | 5440 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0034 | 0/0 | 5445 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0035 | 0/0 | 5440 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0036 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0037 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0038 | 0/0 | 5444 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0039 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0040 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0041 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0042 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0043 | 0/0 | 5451 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0044 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0045 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0046 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0047 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0048 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0049 | 0/0 | 5440 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0050 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| t0051 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| 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 | 4 | 0 | 1 | 0 | 2 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| 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 | 0/1 | 963 | 126 | 39 | 29 | 37 | 7 | 13 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0003 | 0/0 | 963 | 19 | 16 | 3 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0004 | 0/0 | 963 | 4 | 1 | 0 | 2 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0005 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0008 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002 | 0/0 | 963 | 120 | 23 | 19 | 59 | 3 | 16 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0010 | 1/0 | 963 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0003c0006 | 0/0 | 963 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0004c0007 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0005c0009 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0006c0011 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6407 | 16 | 4 | 4 | 2 | 3 | 3 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0002 | 0/0 | 6402 | 26 | 2 | 9 | 8 | 1 | 6 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0003 | 0/0 | 6409 | 15 | 12 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0005 | 0/0 | 6410 | 13 | 0 | 0 | 13 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0008 | 0/1 | 6406 | 8 | 0 | 3 | 0 | 2 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0009 | 0/0 | 6401 | 5 | 5 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0010 | 0/0 | 6402 | 5 | 0 | 0 | 5 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0011 | 0/0 | 6405 | 5 | 5 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0018 | 0/0 | 6410 | 3 | 1 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0019 | 0/0 | 6410 | 3 | 0 | 1 | 0 | 1 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0020 | 0/0 | 6408 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0021 | 0/0 | 6410 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0022 | 0/0 | 6402 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0023 | 0/0 | 6402 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0024 | 0/0 | 6405 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0025 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0026 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0028 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0029 | 0/0 | 6407 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0034 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0035 | 0/0 | 6402 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0036 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0038 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0039 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0040 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0041 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0042 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0045 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0047 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0048 | 0/0 | 6405 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0050 | 0/0 | 6410 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0001t0051 | 0/0 | 6410 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0003t0004 | 0/0 | 6414 | 17 | 15 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0003t0043 | 0/0 | 6413 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0003t0044 | 0/0 | 6414 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0004t0007 | 0/0 | 6402 | 4 | 1 | 0 | 2 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0005t0001 | 0/0 | 6407 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0005t0009 | 0/0 | 6401 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0001c0008t0007 | 0/0 | 6402 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0001 | 0/0 | 6407 | 49 | 7 | 8 | 30 | 1 | 3 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0002 | 0/0 | 6402 | 11 | 1 | 1 | 8 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0003 | 0/0 | 6409 | 11 | 0 | 0 | 9 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0005 | 0/0 | 6410 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0006 | 0/0 | 6406 | 12 | 4 | 2 | 1 | 1 | 4 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0007 | 0/0 | 6402 | 4 | 0 | 0 | 1 | 1 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0008 | 0/0 | 6406 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0010 | 0/0 | 6402 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0012 | 0/0 | 6407 | 4 | 0 | 2 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0013 | 0/0 | 6406 | 4 | 4 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0014 | 0/0 | 6408 | 4 | 0 | 0 | 3 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0015 | 0/0 | 6405 | 3 | 2 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0016 | 0/0 | 6406 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0017 | 0/0 | 6403 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0025 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0027 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0030 | 0/0 | 6407 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0031 | 0/0 | 6407 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0032 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0033 | 0/0 | 6402 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0037 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0002t0049 | 0/0 | 6402 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0002c0010t0004 | 1/0 | 6414 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0003c0006t0007 | 0/0 | 6402 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0004c0007t0003 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0005c0009t0001 | 0/0 | 6407 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| a0006c0011t0046 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | copy fasta | chr10 | 49009236 | 49120522 |
| 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 | 4 | 0 | 1 | 0 | 2 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0010g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0018g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0018g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0019g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0019g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0019g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0020g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0020g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0021g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0021g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0022g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0022g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0023g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0023g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0024g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0024g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0025g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0026g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0028g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0034g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0035g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0036g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0038g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0039g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0040g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0041g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0042g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0045g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0047g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0048g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0050g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0001t0051g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0043g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0003t0044g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0004t0007g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0004t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0004t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0004t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0005t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0005t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0005t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0001c0008t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0010g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0012g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0012g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0013g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0014g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0014g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0015g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0016g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0016g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0016g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0017g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0017g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0025g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0027g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0030g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0031g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0032g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0033g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0037g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0002t0049g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0002c0010t0004g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0003c0006t0007g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0004c0007t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0005c0009t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| a0006c0011t0046g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0197 | EUR | GBR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00280 | hp1 | a0002 | c0002 | t0006 | g0104 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00323 | hp1 | a0002 | c0002 | t0007 | g0101 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00423 | hp1 | a0002 | c0002 | t0010 | g0143 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00438 | hp2 | a0002 | c0002 | t0012 | g0010 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0164 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | CHS | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00639 | hp1 | a0002 | c0002 | t0008 | g0145 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00639 | hp2 | a0001 | c0008 | t0007 | g0020 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00642 | hp1 | a0001 | c0001 | t0024 | g0187 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00642 | hp2 | a0002 | c0002 | t0006 | g0058 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0057 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG00741 | hp2 | a0002 | c0002 | t0031 | g0094 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01069 | hp1 | a0001 | c0001 | t0047 | g0248 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01069 | hp2 | a0001 | c0001 | t0018 | g0169 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0193 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01070 | hp2 | a0001 | c0001 | t0021 | g0241 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0170 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01071 | hp2 | a0001 | c0001 | t0021 | g0242 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01074 | hp1 | a0001 | c0001 | t0048 | g0192 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01081 | hp1 | a0002 | c0002 | t0016 | g0093 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01081 | hp2 | a0001 | c0001 | t0026 | g0195 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01106 | hp1 | a0001 | c0001 | t0028 | g0178 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01109 | hp1 | a0001 | c0003 | t0004 | g0202 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01109 | hp2 | a0002 | c0002 | t0008 | g0133 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0190 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01243 | hp1 | a0001 | c0001 | t0038 | g0198 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01243 | hp2 | a0001 | c0001 | t0024 | g0185 | AMR | PUR | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01346 | hp1 | a0001 | c0001 | t0035 | g0224 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0189 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0186 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01975 | hp1 | a0002 | c0002 | t0016 | g0097 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01978 | hp2 | a0001 | c0001 | t0019 | g0168 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01981 | hp1 | a0001 | c0003 | t0044 | g0201 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01993 | hp2 | a0002 | c0002 | t0012 | g0067 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02056 | hp2 | a0001 | c0001 | t0022 | g0047 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02074 | hp1 | a0002 | c0002 | t0030 | g0041 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0077 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02083 | hp2 | a0001 | c0001 | t0023 | g0033 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02135 | hp2 | a0002 | c0002 | t0033 | g0043 | EAS | KHV | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0200 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02148 | hp1 | a0002 | c0002 | t0012 | g0127 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0173 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02273 | hp2 | a0002 | c0002 | t0016 | g0098 | AMR | PEL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0213 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02572 | hp1 | a0001 | c0005 | t0009 | g0177 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02602 | hp2 | a0002 | c0002 | t0006 | g0089 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02615 | hp2 | a0001 | c0005 | t0009 | g0175 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02622 | hp1 | a0002 | c0002 | t0017 | g0072 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02622 | hp2 | a0002 | c0002 | t0013 | g0008 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0204 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0245 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0209 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02683 | hp2 | a0002 | c0002 | t0032 | g0153 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02698 | hp2 | a0002 | c0002 | t0015 | g0095 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02717 | hp2 | a0001 | c0001 | t0039 | g0167 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02723 | hp1 | a0001 | c0003 | t0004 | g0203 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0239 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02738 | hp1 | a0002 | c0002 | t0006 | g0092 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0025 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02809 | hp2 | a0001 | c0005 | t0009 | g0174 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02818 | hp1 | a0002 | c0002 | t0013 | g0073 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02818 | hp2 | a0001 | c0001 | t0045 | g0249 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02922 | hp1 | a0002 | c0002 | t0015 | g0080 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02922 | hp2 | a0001 | c0003 | t0043 | g0199 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0205 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0246 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02970 | hp1 | a0006 | c0011 | t0046 | g0264 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02970 | hp2 | a0001 | c0003 | t0004 | g0255 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03017 | hp1 | a0002 | c0002 | t0006 | g0124 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03017 | hp2 | a0002 | c0002 | t0006 | g0103 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03041 | hp2 | a0001 | c0004 | t0007 | g0017 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03098 | hp1 | a0001 | c0003 | t0004 | g0206 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0214 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0210 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0256 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03195 | hp1 | a0001 | c0001 | t0042 | g0014 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0029 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03225 | hp1 | a0001 | c0001 | t0025 | g0179 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0212 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03239 | hp2 | a0002 | c0002 | t0007 | g0099 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0176 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0208 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0184 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03486 | hp2 | a0001 | c0001 | t0036 | g0026 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03491 | hp2 | a0003 | c0006 | t0007 | g0005 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03492 | hp2 | a0003 | c0006 | t0007 | g0005 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03516 | hp1 | a0002 | c0002 | t0017 | g0070 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0082 | AFR | ESN | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0171 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03579 | hp2 | a0002 | c0002 | t0006 | g0078 | AFR | MSL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03654 | hp2 | a0002 | c0002 | t0007 | g0091 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0163 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0196 | SAS | PJL | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03927 | hp2 | a0002 | c0002 | t0014 | g0123 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03942 | hp1 | a0001 | c0004 | t0007 | g0016 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | BEB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0155 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG04199 | hp2 | a0002 | c0002 | t0049 | g0151 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0161 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG04204 | hp2 | a0001 | c0001 | t0034 | g0234 | SAS | STU | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | CHB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | CHB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18941 | hp1 | a0001 | c0004 | t0007 | g0019 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18941 | hp2 | a0001 | c0001 | t0051 | g0054 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18944 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18965 | hp1 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18965 | hp2 | a0002 | c0002 | t0027 | g0117 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18967 | hp2 | a0001 | c0001 | t0010 | g0228 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18970 | hp1 | a0001 | c0001 | t0050 | g0053 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18977 | hp1 | a0002 | c0002 | t0014 | g0134 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18979 | hp2 | a0002 | c0002 | t0014 | g0102 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18983 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18984 | hp1 | a0002 | c0002 | t0012 | g0010 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18985 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18985 | hp2 | a0002 | c0002 | t0006 | g0160 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18994 | hp1 | a0005 | c0009 | t0001 | g0038 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19002 | hp1 | a0001 | c0001 | t0022 | g0045 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19002 | hp2 | a0002 | c0002 | t0005 | g0120 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19003 | hp1 | a0004 | c0007 | t0003 | g0154 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19030 | hp1 | a0002 | c0002 | t0037 | g0083 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19030 | hp2 | a0002 | c0002 | t0025 | g0146 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19058 | hp2 | a0001 | c0004 | t0007 | g0056 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19062 | hp2 | a0001 | c0001 | t0023 | g0046 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19085 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19240 | hp1 | a0002 | c0002 | t0015 | g0076 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA19240 | hp2 | a0001 | c0003 | t0004 | g0172 | AFR | YRI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | ASW | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20129 | hp2 | a0002 | c0002 | t0017 | g0071 | AFR | ASW | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0191 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20752 | hp2 | a0001 | c0001 | t0019 | g0181 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0233 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0115 | EUR | TSI | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | GIH | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20905 | hp2 | a0001 | c0001 | t0019 | g0180 | SAS | GIH | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01123 | hp1 | a0001 | c0003 | t0004 | g0215 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0211 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02109 | hp2 | a0002 | c0002 | t0006 | g0100 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02486 | hp2 | a0002 | c0002 | t0013 | g0008 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02559 | hp1 | a0002 | c0002 | t0006 | g0079 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| HG06807 | hp2 | a0002 | c0002 | t0013 | g0074 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18955 | hp1 | a0002 | c0002 | t0014 | g0129 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA21309 | hp1 | a0002 | c0002 | t0006 | g0086 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| NA21309 | hp2 | a0001 | c0001 | t0041 | g0247 | AFR | LWK | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0194 | REF | REF | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| homoSapiens_grch38 | hp1 | a0002 | c0010 | t0004 | g0105 | REF | REF | VSTM4_chr10_49009236_49120522 | VSTM4 | chr10 | 49009236 | 49120522 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49077267
|
T | G | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.586A>C | p.Met196Leu | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/8 | 623/6414 | 586/963 | 196/320 | chr10 | 49077267 | ||
| chr10:49107734
|
C | T | 1 | a0005 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.317G>A | p.Arg106Gln | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 354/6414 | 317/963 | 106/320 | chr10 | 49107734 | ||
| chr10:49107848
|
A | G | 3 | a0001a0003a0006 | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
missense_variant | MODERATE | c.203T>C | p.Phe68Ser | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 240/6414 | 203/963 | 68/320 | chr10 | 49107848 | ||
| chr10:49107893
|
C | T | 1 | a0004 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.158G>A | p.Arg53Gln | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 195/6414 | 158/963 | 53/320 | chr10 | 49107893 | ||
| chr10:49115463
|
G | A | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.23C>T | p.Ala8Val | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/8 | 60/6414 | 23/963 | 8/320 | chr10 | 49115463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49019740
|
T | C | 9 | a0001c0001a0001c0004a0001c0005others(6): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
synonymous_variant | LOW | c.873A>G | p.Glu291Glu | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 910/6414 | 873/963 | 291/320 | chr10 | 49019740 | ||
| chr10:49048503
|
G | A | 3 | a0001c0004a0001c0008a0003c0006 | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
synonymous_variant | LOW | c.750C>T | p.Asp250Asp | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/8 | 787/6414 | 750/963 | 250/320 | chr10 | 49048503 | ||
| chr10:49107676
|
G | A | 2 | a0001c0008a0006c0011 | 2 | HG00639.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.375C>T | p.Tyr125Tyr | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 412/6414 | 375/963 | 125/320 | chr10 | 49107676 | ||
| chr10:49107772
|
G | A | 1 | a0001c0005 | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.279C>T | p.Ser93Ser | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/8 | 316/6414 | 279/963 | 93/320 | chr10 | 49107772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49014382
|
T | C | 3 | a0001c0001t0018a0001c0001t0019a0001c0001t0021 | 8 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5268A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5268 | chr10 | 49014382 | |||||
| chr10:49014516
|
C | T | 1 | a0001c0001t0051 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5134 | chr10 | 49014516 | |||||
| chr10:49014516
|
CCT | C | 20 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(17): Show | 76 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5132_*5133delAG | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5132 | chr10 | 49014516 | |||||
| chr10:49014540
|
G | T | 23 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(20): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*5110C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5110 | chr10 | 49014540 | |||||
| chr10:49014609
|
GTT | G | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(50): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*5039_*5040delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 5039 | chr10 | 49014609 | |||||
| chr10:49014724
|
T | G | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(50): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*4926A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4926 | chr10 | 49014724 | |||||
| chr10:49014953
|
G | A | 2 | a0001c0001t0011a0001c0001t0024 | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4697C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4697 | chr10 | 49014953 | |||||
| chr10:49015020
|
A | G | 4 | a0001c0001t0005a0001c0001t0050a0001c0001t0051others(1): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4630T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4630 | chr10 | 49015020 | |||||
| chr10:49015118
|
CATT | C | 2 | a0001c0001t0011a0001c0001t0024 | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4531delAAT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4529 | chr10 | 49015118 | |||||
| chr10:49015119
|
A | ATT | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0019others(5): Show | 25 | HG00423.hp2 HG01069.hp2 HG01070.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4530dupAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4530 | chr10 | 49015119 | |||||
| chr10:49015119
|
AT | A | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0028others(15): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*4530delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4530 | chr10 | 49015119 | |||||
| chr10:49015119
|
ATT | A | 7 | a0001c0001t0008a0001c0001t0026a0001c0001t0038others(4): Show | 28 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4529_*4530delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4529 | chr10 | 49015119 | |||||
| chr10:49015119
|
ATTT | A | 4 | a0001c0001t0036a0001c0001t0048a0002c0002t0015others(1): Show | 8 | HG01074.hp1 HG02622.hp1 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4528_*4530delAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4528 | chr10 | 49015119 | |||||
| chr10:49015119
|
ATTTT | A | 18 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(15): Show | 72 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4527_*4530delAAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4527 | chr10 | 49015119 | |||||
| chr10:49015122
|
T | G | 2 | a0001c0001t0011a0001c0001t0024 | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4528A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4528 | chr10 | 49015122 | |||||
| chr10:49015144
|
C | G | 1 | a0001c0001t0018 | 3 | HG01069.hp2 HG01071.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4506G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4506 | chr10 | 49015144 | |||||
| chr10:49015368
|
G | A | 2 | a0001c0001t0011a0001c0001t0024 | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4282C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4282 | chr10 | 49015368 | |||||
| chr10:49015411
|
G | A | 4 | a0001c0004t0007a0001c0008t0007a0002c0002t0007others(1): Show | 11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4239C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4239 | chr10 | 49015411 | |||||
| chr10:49015454
|
G | C | 1 | a0001c0003t0044 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4196C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4196 | chr10 | 49015454 | |||||
| chr10:49015478
|
G | A | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4172C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4172 | chr10 | 49015478 | |||||
| chr10:49015481
|
C | T | 3 | a0001c0001t0018a0001c0001t0019a0001c0001t0021 | 8 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4169G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4169 | chr10 | 49015481 | |||||
| chr10:49015569
|
G | A | 24 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(21): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4081C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 4081 | chr10 | 49015569 | |||||
| chr10:49015792
|
G | A | 8 | a0001c0001t0003a0001c0001t0025a0001c0001t0045others(5): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3858C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3858 | chr10 | 49015792 | |||||
| chr10:49015849
|
C | T | 1 | a0001c0001t0050 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3801G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3801 | chr10 | 49015849 | |||||
| chr10:49015851
|
C | T | 1 | a0001c0001t0028 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3799G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3799 | chr10 | 49015851 | |||||
| chr10:49015862
|
C | T | 1 | a0001c0001t0039 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3788G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3788 | chr10 | 49015862 | |||||
| chr10:49016027
|
C | G | 1 | a0001c0001t0020 | 2 | HG02630.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3623G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3623 | chr10 | 49016027 | |||||
| chr10:49016090
|
T | C | 1 | a0006c0011t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3560A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3560 | chr10 | 49016090 | |||||
| chr10:49016118
|
TTTTG | T | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*3528_*3531delCAAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3528 | chr10 | 49016118 | |||||
| chr10:49016359
|
G | T | 21 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(18): Show | 77 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3291C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 3291 | chr10 | 49016359 | |||||
| chr10:49016710
|
C | T | 1 | a0002c0002t0033 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2940 | chr10 | 49016710 | |||||
| chr10:49016721
|
C | T | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0026others(17): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2929G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2929 | chr10 | 49016721 | |||||
| chr10:49016740
|
C | T | 1 | a0001c0001t0022 | 2 | HG02056.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2910G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2910 | chr10 | 49016740 | |||||
| chr10:49016811
|
C | T | 23 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(20): Show | 80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2839G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2839 | chr10 | 49016811 | |||||
| chr10:49016989
|
C | G | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2661G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2661 | chr10 | 49016989 | |||||
| chr10:49017018
|
T | C | 10 | a0001c0001t0009a0001c0001t0036a0001c0001t0039others(7): Show | 25 | HG00323.hp1 HG00639.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2632A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2632 | chr10 | 49017018 | |||||
| chr10:49017077
|
CA | C | 1 | a0002c0002t0013 | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2572delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2572 | chr10 | 49017077 | |||||
| chr10:49017406
|
T | C | 1 | a0001c0001t0047 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2244A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2244 | chr10 | 49017406 | |||||
| chr10:49017421
|
G | A | 1 | a0001c0001t0035 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2229 | chr10 | 49017421 | |||||
| chr10:49017425
|
A | G | 11 | a0001c0001t0009a0001c0001t0036a0001c0001t0038others(8): Show | 26 | HG00323.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2225T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2225 | chr10 | 49017425 | |||||
| chr10:49017437
|
A | G | 2 | a0001c0001t0025a0002c0002t0025 | 2 | HG03225.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2213T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2213 | chr10 | 49017437 | |||||
| chr10:49017531
|
T | C | 1 | a0001c0001t0024 | 2 | HG00642.hp1 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2119A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2119 | chr10 | 49017531 | |||||
| chr10:49017598
|
G | C | 8 | a0001c0001t0003a0001c0001t0025a0001c0001t0045others(5): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2052C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2052 | chr10 | 49017598 | |||||
| chr10:49017624
|
T | C | 1 | a0002c0002t0030 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2026A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2026 | chr10 | 49017624 | |||||
| chr10:49017629
|
G | A | 2 | a0001c0001t0022a0001c0001t0023 | 4 | HG02056.hp2 HG02083.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2021C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 2021 | chr10 | 49017629 | |||||
| chr10:49017690
|
G | A | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0026others(17): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1960 | chr10 | 49017690 | |||||
| chr10:49017709
|
C | T | 22 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(19): Show | 79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1941G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1941 | chr10 | 49017709 | |||||
| chr10:49017829
|
T | C | 1 | a0002c0002t0031 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1821 | chr10 | 49017829 | |||||
| chr10:49017834
|
T | C | 4 | a0001c0004t0007a0001c0008t0007a0002c0002t0007others(1): Show | 11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1816A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1816 | chr10 | 49017834 | |||||
| chr10:49018186
|
T | C | 1 | a0002c0002t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1464 | chr10 | 49018186 | |||||
| chr10:49018258
|
A | G | 1 | a0002c0002t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1392 | chr10 | 49018258 | |||||
| chr10:49018289
|
T | G | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0026others(17): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1361 | chr10 | 49018289 | |||||
| chr10:49018540
|
C | T | 2 | a0001c0001t0010a0002c0002t0010 | 6 | HG00423.hp1 NA18944.hp1 NA18965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1110 | chr10 | 49018540 | |||||
| chr10:49018549
|
A | G | 6 | a0001c0001t0005a0001c0001t0041a0001c0001t0042others(3): Show | 18 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1101T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 1101 | chr10 | 49018549 | |||||
| chr10:49018673
|
CA | C | 3 | a0001c0001t0009a0001c0001t0036a0001c0005t0009 | 9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*976delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 976 | chr10 | 49018673 | |||||
| chr10:49018759
|
C | A | 4 | a0001c0001t0008a0001c0001t0026a0001c0001t0048others(1): Show | 12 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 891 | chr10 | 49018759 | |||||
| chr10:49018807
|
T | C | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*843A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 843 | chr10 | 49018807 | |||||
| chr10:49019084
|
C | T | 23 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(20): Show | 80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*566G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 566 | chr10 | 49019084 | |||||
| chr10:49019246
|
C | G | 1 | a0002c0002t0027 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 404 | chr10 | 49019246 | |||||
| chr10:49019278
|
A | G | 11 | a0001c0001t0002a0001c0001t0010a0001c0001t0021others(8): Show | 53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*372T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 372 | chr10 | 49019278 | |||||
| chr10:49019339
|
G | A | 1 | a0002c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 311 | chr10 | 49019339 | |||||
| chr10:49019363
|
G | A | 2 | a0002c0002t0016a0002c0002t0032 | 4 | HG01081.hp1 HG01975.hp1 HG02273.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*287C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 287 | chr10 | 49019363 | |||||
| chr10:49019411
|
G | A | 4 | a0001c0001t0005a0001c0001t0050a0001c0001t0051others(1): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*239C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 239 | chr10 | 49019411 | |||||
| chr10:49019431
|
C | T | 1 | a0001c0001t0020 | 2 | HG02630.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 219 | chr10 | 49019431 | |||||
| chr10:49019470
|
C | T | 16 | a0001c0001t0001a0001c0001t0028a0001c0001t0029others(13): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*180G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 180 | chr10 | 49019470 | |||||
| chr10:49019514
|
C | T | 2 | a0002c0002t0012a0002c0002t0027 | 5 | HG00438.hp2 HG01993.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 136 | chr10 | 49019514 | |||||
| chr10:49019538
|
C | T | 1 | a0001c0001t0026 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 8/8 | 112 | chr10 | 49019538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49019825
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(212): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.838-50G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49019825 | ||||||
| chr10:49019882
|
C | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(241): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.838-107G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49019882 | ||||||
| chr10:49020060
|
C | T | 1 | a0002c0002t0013g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.838-285G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020060 | ||||||
| chr10:49020221
|
C | T | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.838-446G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020221 | ||||||
| chr10:49020530
|
AC | A | 13 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-756delG | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020530 | ||||||
| chr10:49020568
|
A | G | 2 | a0001c0004t0007g0019a0001c0004t0007g0056 | 2 | NA18941.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.838-793T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020568 | ||||||
| chr10:49020703
|
A | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(92): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.838-928T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020703 | ||||||
| chr10:49020727
|
A | AGAAG | 100 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(97): Show | 107 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.838-956_838-953dup others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020727
|
A | AGGAAG | 3 | a0001c0005t0001g0176a0002c0002t0006g0104a0002c0002t0015g0076 | 3 | HG00280.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.838-953_838-952ins others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020727
|
A | AGGAAGGA others(2): Show |
40 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 43 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(9): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020727
|
A | AGGAAGGA others(6): Show |
45 | a0001c0001t0026g0195a0002c0002t0001g0009a0002c0002t0001g0039others(42): Show | 46 | HG00597.hp2 HG00621.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020727
|
A | AGGAAGGA others(10): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0221others(16): Show | 23 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.838-953_838-952ins others(17): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020727
|
AGAAG | A | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-956_838-953del others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020727 | ||||||
| chr10:49020743
|
G | A | 2 | a0001c0001t0020g0245a0001c0001t0020g0256 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.838-968C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020743 | ||||||
| chr10:49020753
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(106): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.838-978C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020753 | ||||||
| chr10:49020757
|
G | A | 7 | a0001c0001t0001g0034a0002c0002t0001g0002a0002c0002t0001g0106others(4): Show | 9 | HG01106.hp2 HG02027.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-982C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020757 | ||||||
| chr10:49020835
|
G | C | 1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.838-1060C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020835 | ||||||
| chr10:49020871
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-1096C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020871 | ||||||
| chr10:49020877
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-1102A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49020877 | ||||||
| chr10:49021038
|
A | C | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-1263T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021038 | ||||||
| chr10:49021151
|
C | CCTAAAAG others(2228): Show |
1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.838-1377_838-1376i others(2237): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021151 | ||||||
| chr10:49021151
|
C | CCTAAAAG others(2235): Show |
1 | a0001c0001t0020g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.838-1377_838-1376i others(2244): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021151 | ||||||
| chr10:49021204
|
GA | G | 10 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(7): Show | 11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-1430delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021204 | ||||||
| chr10:49021445
|
A | T | 2 | a0001c0003t0004g0211a0001c0003t0004g0213 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.838-1670T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021445 | ||||||
| chr10:49021493
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(228): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.838-1718T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021493 | ||||||
| chr10:49021593
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-1818A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021593 | ||||||
| chr10:49021620
|
C | T | 3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.838-1845G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021620 | ||||||
| chr10:49021709
|
T | G | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.838-1934A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021709 | ||||||
| chr10:49021717
|
A | G | 1 | a0002c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.838-1942T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021717 | ||||||
| chr10:49021921
|
T | C | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-2146A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021921 | ||||||
| chr10:49021976
|
C | T | 2 | a0001c0001t0002g0233a0002c0002t0002g0096 | 2 | HG01952.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.838-2201G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49021976 | ||||||
| chr10:49022082
|
A | C | 12 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-2307T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022082 | ||||||
| chr10:49022111
|
T | A | 1 | a0002c0002t0015g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.838-2336A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022111 | ||||||
| chr10:49022118
|
TTTA | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(70): Show | 78 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.838-2346_838-2344d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022118 | ||||||
| chr10:49022121
|
A | AT | 10 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(7): Show | 10 | HG00099.hp1 HG00639.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-2347dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022121 | ||||||
| chr10:49022195
|
T | C | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-2420A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022195 | ||||||
| chr10:49022293
|
G | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(248): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.838-2518C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022293 | ||||||
| chr10:49022302
|
A | T | 12 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-2527T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022302 | ||||||
| chr10:49022471
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.838-2696T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022471 | ||||||
| chr10:49022473
|
A | C | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-2698T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022473 | ||||||
| chr10:49022705
|
T | C | 1 | a0001c0001t0009g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.838-2930A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022705 | ||||||
| chr10:49022878
|
C | T | 3 | a0001c0001t0011g0188a0001c0001t0011g0205a0001c0001t0024g0187 | 3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.838-3103G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022878 | ||||||
| chr10:49022981
|
C | T | 2 | a0001c0001t0009g0030a0001c0001t0009g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.838-3206G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49022981 | ||||||
| chr10:49023110
|
T | C | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-3335A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023110 | ||||||
| chr10:49023127
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01192.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.838-3352A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023127 | ||||||
| chr10:49023139
|
A | G | 1 | a0002c0002t0006g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.838-3364T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023139 | ||||||
| chr10:49023270
|
T | C | 1 | a0002c0002t0007g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.838-3495A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023270 | ||||||
| chr10:49023305
|
A | G | 1 | a0001c0001t0028g0178 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.838-3530T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023305 | ||||||
| chr10:49023407
|
G | A | 1 | a0002c0002t0003g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.838-3632C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023407 | ||||||
| chr10:49023509
|
T | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.838-3734A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023509 | ||||||
| chr10:49023623
|
C | A | 1 | a0001c0001t0002g0222 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.838-3848G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023623 | ||||||
| chr10:49023684
|
C | G | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.838-3909G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023684 | ||||||
| chr10:49023738
|
T | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-3963A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023738 | ||||||
| chr10:49023739
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-3964C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023739 | ||||||
| chr10:49023795
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(118): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.838-4020G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023795 | ||||||
| chr10:49023824
|
G | T | 1 | a0002c0002t0006g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.838-4049C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023824 | ||||||
| chr10:49023827
|
G | A | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.838-4052C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023827 | ||||||
| chr10:49023835
|
G | A | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-4060C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023835 | ||||||
| chr10:49023837
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0045g0249 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.838-4062A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49023837 | ||||||
| chr10:49024074
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.838-4299A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024074 | ||||||
| chr10:49024134
|
C | T | 3 | a0001c0001t0002g0220a0001c0001t0002g0244a0002c0002t0002g0155 | 3 | HG02615.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.838-4359G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024134 | ||||||
| chr10:49024135
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(212): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.838-4360T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024135 | ||||||
| chr10:49024195
|
CT | C | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-4421delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024195 | ||||||
| chr10:49024241
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-4466A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024241 | ||||||
| chr10:49024367
|
G | C | 35 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(32): Show | 36 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.838-4592C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024367 | ||||||
| chr10:49024381
|
C | T | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.838-4606G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024381 | ||||||
| chr10:49024440
|
A | G | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.838-4665T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024440 | ||||||
| chr10:49024496
|
G | C | 1 | a0002c0002t0002g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.838-4721C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024496 | ||||||
| chr10:49024811
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.838-5036G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024811 | ||||||
| chr10:49024827
|
C | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-5052G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024827 | ||||||
| chr10:49024838
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-5063G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024838 | ||||||
| chr10:49024944
|
GT | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-5170delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024944 | ||||||
| chr10:49024959
|
T | C | 6 | a0001c0001t0018g0169a0001c0001t0018g0170a0001c0001t0018g0171others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-5184A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49024959 | ||||||
| chr10:49025076
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-5301G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025076 | ||||||
| chr10:49025232
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.838-5457C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025232 | ||||||
| chr10:49025429
|
T | C | 13 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-5654A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025429 | ||||||
| chr10:49025476
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.838-5701G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025476 | ||||||
| chr10:49025524
|
C | T | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-5749G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025524 | ||||||
| chr10:49025538
|
C | T | 1 | a0001c0003t0004g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838-5763G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025538 | ||||||
| chr10:49025552
|
T | C | 1 | a0002c0002t0017g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.838-5777A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025552 | ||||||
| chr10:49025794
|
G | A | 1 | a0001c0001t0008g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.838-6019C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025794 | ||||||
| chr10:49025932
|
C | T | 74 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(71): Show | 79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.838-6157G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49025932 | ||||||
| chr10:49026034
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0020g0245a0001c0001t0020g0256 | 3 | HG02145.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.838-6259G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026034 | ||||||
| chr10:49026300
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-6525G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026300 | ||||||
| chr10:49026355
|
T | C | 78 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(75): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.838-6580A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026355 | ||||||
| chr10:49026356
|
G | A | 1 | a0002c0002t0037g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838-6581C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026356 | ||||||
| chr10:49026376
|
T | C | 50 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(47): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.838-6601A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026376 | ||||||
| chr10:49026492
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-6717C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026492 | ||||||
| chr10:49026618
|
G | T | 2 | a0002c0002t0012g0067a0002c0002t0012g0127 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.838-6843C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026618 | ||||||
| chr10:49026841
|
C | T | 16 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(13): Show | 18 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.838-7066G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026841 | ||||||
| chr10:49026990
|
A | C | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-7215T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026990 | ||||||
| chr10:49026999
|
G | A | 3 | a0001c0001t0005g0061a0001c0001t0005g0062a0001c0001t0005g0063 | 3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.838-7224C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49026999 | ||||||
| chr10:49027087
|
T | C | 1 | a0002c0002t0001g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.838-7312A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027087 | ||||||
| chr10:49027290
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-7515C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027290 | ||||||
| chr10:49027467
|
T | C | 1 | a0001c0005t0009g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.838-7692A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027467 | ||||||
| chr10:49027574
|
C | T | 49 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(46): Show | 53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.838-7799G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027574 | ||||||
| chr10:49027590
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0087others(74): Show | 84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.838-7815G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027590 | ||||||
| chr10:49027653
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.838-7878T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027653 | ||||||
| chr10:49027670
|
A | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(241): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.838-7895T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027670 | ||||||
| chr10:49027786
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.838-8011G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027786 | ||||||
| chr10:49027893
|
G | C | 1 | a0001c0008t0007g0020 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.838-8118C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49027893 | ||||||
| chr10:49028135
|
C | T | 1 | a0002c0002t0015g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.838-8360G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028135 | ||||||
| chr10:49028323
|
C | A | 1 | a0001c0001t0009g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838-8548G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028323 | ||||||
| chr10:49028323
|
C | T | 12 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-8548G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028323 | ||||||
| chr10:49028435
|
C | A | 77 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-8660G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028435 | ||||||
| chr10:49028534
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(180): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.838-8759A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028534 | ||||||
| chr10:49028584
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-8809A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028584 | ||||||
| chr10:49028586
|
G | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-8811C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028586 | ||||||
| chr10:49028644
|
T | C | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-8869A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028644 | ||||||
| chr10:49028847
|
T | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-9072A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49028847 | ||||||
| chr10:49029143
|
A | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-9368T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029143 | ||||||
| chr10:49029394
|
G | A | 1 | a0001c0003t0004g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.838-9619C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029394 | ||||||
| chr10:49029415
|
C | A | 1 | a0001c0003t0004g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.838-9640G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029415 | ||||||
| chr10:49029562
|
C | T | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-9787G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029562 | ||||||
| chr10:49029715
|
G | T | 1 | a0002c0002t0037g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838-9940C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029715 | ||||||
| chr10:49029739
|
C | T | 12 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-9964G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029739 | ||||||
| chr10:49029775
|
G | C | 1 | a0001c0003t0044g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.838-10000C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49029775 | ||||||
| chr10:49030072
|
G | A | 77 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-10297C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030072 | ||||||
| chr10:49030137
|
A | G | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.838-10362T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030137 | ||||||
| chr10:49030227
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-10452G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030227 | ||||||
| chr10:49030234
|
C | A | 2 | a0002c0002t0007g0099a0002c0002t0007g0101 | 2 | HG00323.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.838-10459G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030234 | ||||||
| chr10:49030309
|
C | T | 1 | a0002c0002t0006g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.838-10534G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030309 | ||||||
| chr10:49030310
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-10535T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030310 | ||||||
| chr10:49030408
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.838-10633T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030408 | ||||||
| chr10:49030525
|
C | T | 70 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(67): Show | 75 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.838-10750G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030525 | ||||||
| chr10:49030618
|
C | T | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-10843G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030618 | ||||||
| chr10:49030633
|
T | C | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838-10858A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030633 | ||||||
| chr10:49030648
|
C | T | 1 | a0001c0003t0004g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838-10873G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030648 | ||||||
| chr10:49030654
|
A | T | 13 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-10879T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030654 | ||||||
| chr10:49030829
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-11054A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030829 | ||||||
| chr10:49030874
|
A | G | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-11099T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030874 | ||||||
| chr10:49030917
|
G | C | 1 | a0002c0002t0001g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.838-11142C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49030917 | ||||||
| chr10:49031008
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0087others(78): Show | 88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.838-11233A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031008 | ||||||
| chr10:49031096
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.838-11321A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031096 | ||||||
| chr10:49031116
|
T | C | 77 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-11341A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031116 | ||||||
| chr10:49031200
|
C | G | 32 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.838-11425G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031200 | ||||||
| chr10:49031209
|
C | T | 2 | a0002c0002t0002g0156a0002c0002t0002g0157 | 2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.838-11434G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031209 | ||||||
| chr10:49031430
|
A | G | 77 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-11655T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031430 | ||||||
| chr10:49031450
|
C | T | 4 | a0001c0001t0040g0173a0002c0002t0017g0070a0002c0002t0017g0071others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-11675G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031450 | ||||||
| chr10:49031798
|
C | T | 4 | a0001c0001t0002g0182a0001c0001t0021g0241a0001c0001t0021g0242others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-12023G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031798 | ||||||
| chr10:49031885
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-12110G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031885 | ||||||
| chr10:49031891
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.838-12116T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031891 | ||||||
| chr10:49031952
|
C | G | 77 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(74): Show | 82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.838-12177G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49031952 | ||||||
| chr10:49032120
|
A | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(213): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.838-12345T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032120 | ||||||
| chr10:49032163
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(213): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.838-12388G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032163 | ||||||
| chr10:49032195
|
G | T | 3 | a0001c0001t0025g0179a0001c0001t0041g0247a0002c0002t0025g0146 | 3 | HG03225.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.838-12420C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032195 | ||||||
| chr10:49032234
|
C | T | 1 | a0002c0002t0032g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.838-12459G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032234 | ||||||
| chr10:49032264
|
G | A | 13 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-12489C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032264 | ||||||
| chr10:49032294
|
T | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(241): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.838-12519A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032294 | ||||||
| chr10:49032316
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-12541A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032316 | ||||||
| chr10:49032493
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.838-12718T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032493 | ||||||
| chr10:49032517
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0020g0245 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.838-12742C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032517 | ||||||
| chr10:49032572
|
A | C | 1 | a0001c0001t0018g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.838-12797T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032572 | ||||||
| chr10:49032767
|
C | T | 1 | a0002c0002t0006g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.838-12992G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032767 | ||||||
| chr10:49032872
|
C | CAG | 7 | a0001c0001t0008g0189a0001c0001t0008g0191a0001c0001t0008g0194others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-13099_838-1309 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032872 | ||||||
| chr10:49032909
|
G | A | 4 | a0001c0001t0040g0173a0002c0002t0017g0070a0002c0002t0017g0071others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-13134C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032909 | ||||||
| chr10:49032938
|
CT | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(104): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.838-13164delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49032938 | ||||||
| chr10:49033277
|
A | G | 13 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-13502T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033277 | ||||||
| chr10:49033293
|
A | G | 10 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(7): Show | 11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-13518T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033293 | ||||||
| chr10:49033359
|
T | C | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.838-13584A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033359 | ||||||
| chr10:49033492
|
G | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+13491C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033492 | ||||||
| chr10:49033743
|
C | T | 1 | a0001c0004t0007g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+13240G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033743 | ||||||
| chr10:49033745
|
G | C | 1 | a0002c0002t0037g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+13238C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033745 | ||||||
| chr10:49033893
|
C | T | 78 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(75): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13090G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033893 | ||||||
| chr10:49033962
|
TCAC | T | 78 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(75): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13018_837+1302 others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033962 | ||||||
| chr10:49033970
|
A | T | 78 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(75): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+13013T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49033970 | ||||||
| chr10:49034157
|
C | T | 1 | a0001c0004t0007g0019 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.837+12826G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034157 | ||||||
| chr10:49034190
|
CCACCATC others(2): Show |
C | 105 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(102): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.837+12784_837+1279 others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034190 | ||||||
| chr10:49034275
|
T | C | 75 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(72): Show | 80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.837+12708A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034275 | ||||||
| chr10:49034362
|
G | A | 1 | a0002c0002t0006g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.837+12621C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034362 | ||||||
| chr10:49034404
|
C | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(249): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.837+12579G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034404 | ||||||
| chr10:49034462
|
C | T | 9 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(6): Show | 9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+12521G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034462 | ||||||
| chr10:49034465
|
T | A | 3 | a0001c0001t0011g0188a0001c0001t0011g0205a0001c0001t0024g0187 | 3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.837+12518A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034465 | ||||||
| chr10:49034736
|
C | T | 1 | a0002c0002t0006g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837+12247G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034736 | ||||||
| chr10:49034763
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(102): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.837+12220A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49034763 | ||||||
| chr10:49035066
|
C | T | 3 | a0001c0001t0011g0188a0001c0001t0011g0205a0001c0001t0024g0187 | 3 | HG00642.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.837+11917G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035066 | ||||||
| chr10:49035067
|
G | A | 17 | a0001c0001t0003g0032a0001c0001t0003g0036a0001c0001t0003g0217others(14): Show | 17 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.837+11916C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035067 | ||||||
| chr10:49035192
|
C | T | 14 | a0001c0001t0001g0221a0002c0002t0001g0260a0002c0002t0006g0057others(11): Show | 14 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.837+11791G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035192 | ||||||
| chr10:49035254
|
T | A | 3 | a0001c0001t0003g0257a0001c0001t0003g0259a0001c0001t0020g0256 | 3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.837+11729A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035254 | ||||||
| chr10:49035291
|
A | C | 50 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(47): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+11692T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035291 | ||||||
| chr10:49035346
|
G | T | 78 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(75): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.837+11637C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035346 | ||||||
| chr10:49035448
|
G | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.837+11535C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035448 | ||||||
| chr10:49035462
|
G | A | 1 | a0002c0002t0037g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+11521C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035462 | ||||||
| chr10:49035494
|
C | T | 79 | a0001c0001t0001g0013a0001c0001t0002g0003a0001c0001t0002g0015others(76): Show | 84 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.837+11489G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035494 | ||||||
| chr10:49035553
|
G | A | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837+11430C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035553 | ||||||
| chr10:49035657
|
A | C | 10 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(7): Show | 11 | HG00323.hp1 HG00639.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+11326T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035657 | ||||||
| chr10:49035669
|
C | CA | 54 | a0001c0001t0001g0023a0001c0001t0003g0011a0001c0001t0003g0018others(51): Show | 57 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.837+11313dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | ||||||
| chr10:49035669
|
C | CAA | 168 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(165): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.837+11312_837+1131 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | ||||||
| chr10:49035669
|
C | CAAA | 14 | a0001c0001t0002g0227a0001c0004t0007g0056a0001c0008t0007g0020others(11): Show | 14 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+11311_837+1131 others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035669 | ||||||
| chr10:49035687
|
A | AAAAAAAA others(3): Show |
3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.837+11295_837+1129 others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035687 | ||||||
| chr10:49035722
|
C | A | 1 | a0002c0002t0003g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.837+11261G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035722 | ||||||
| chr10:49035723
|
A | G | 1 | a0002c0002t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.837+11260T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035723 | ||||||
| chr10:49035788
|
C | T | 3 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0024g0185 | 3 | HG01243.hp2 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.837+11195G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035788 | ||||||
| chr10:49035915
|
G | T | 50 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0035others(47): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+11068C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035915 | ||||||
| chr10:49035988
|
G | C | 1 | a0001c0001t0002g0182 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.837+10995C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49035988 | ||||||
| chr10:49036103
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(170): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.837+10880T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036103 | ||||||
| chr10:49036118
|
C | T | 4 | a0002c0002t0006g0078a0002c0002t0006g0086a0002c0002t0015g0076others(1): Show | 4 | HG02922.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+10865G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036118 | ||||||
| chr10:49036123
|
A | G | 31 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0032others(28): Show | 32 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.837+10860T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036123 | ||||||
| chr10:49036138
|
G | A | 12 | a0002c0002t0001g0260a0002c0002t0006g0057a0002c0002t0006g0058others(9): Show | 12 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+10845C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036138 | ||||||
| chr10:49036197
|
G | A | 1 | a0001c0003t0004g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.837+10786C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036197 | ||||||
| chr10:49036228
|
C | T | 3 | a0001c0001t0008g0193a0001c0001t0008g0196a0001c0001t0048g0192 | 3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.837+10755G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036228 | ||||||
| chr10:49036326
|
G | A | 9 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0011g0188others(6): Show | 10 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+10657C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036326 | ||||||
| chr10:49036605
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+10378C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036605 | ||||||
| chr10:49036757
|
A | G | 1 | a0002c0002t0037g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837+10226T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036757 | ||||||
| chr10:49036779
|
G | C | 4 | a0002c0002t0006g0078a0002c0002t0006g0086a0002c0002t0015g0076others(1): Show | 4 | HG02922.hp1 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+10204C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49036779 | ||||||
| chr10:49037437
|
A | G | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+9546T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037437 | ||||||
| chr10:49037512
|
T | C | 21 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(18): Show | 21 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.837+9471A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037512 | ||||||
| chr10:49037518
|
T | C | 10 | a0002c0002t0003g0109a0002c0002t0003g0158a0002c0002t0003g0159others(7): Show | 10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+9465A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037518 | ||||||
| chr10:49037531
|
C | A | 16 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0250others(13): Show | 17 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.837+9452G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037531 | ||||||
| chr10:49037562
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+9421T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037562 | ||||||
| chr10:49037936
|
C | CA | 14 | a0001c0001t0002g0182a0001c0001t0002g0218a0001c0001t0003g0217others(11): Show | 14 | HG00558.hp2 HG01071.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.837+9046dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037936 | ||||||
| chr10:49037940
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(240): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.837+9043C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49037940 | ||||||
| chr10:49038021
|
T | C | 3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.837+8962A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038021 | ||||||
| chr10:49038524
|
G | A | 1 | a0001c0001t0047g0248 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.837+8459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038524 | ||||||
| chr10:49038643
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+8340C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038643 | ||||||
| chr10:49038793
|
A | T | 26 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(23): Show | 28 | HG00423.hp2 HG00558.hp1 HG02723.hp2 others(25): Show |
intron_variant | MODIFIER | c.837+8190T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038793 | ||||||
| chr10:49038834
|
C | T | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+8149G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038834 | ||||||
| chr10:49038965
|
C | G | 24 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(21): Show | 25 | HG01069.hp1 HG01070.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.837+8018G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49038965 | ||||||
| chr10:49039076
|
C | A | 10 | a0002c0002t0003g0109a0002c0002t0003g0158a0002c0002t0003g0159others(7): Show | 10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+7907G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039076 | ||||||
| chr10:49039206
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(99): Show | 110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.837+7777C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039206 | ||||||
| chr10:49039247
|
C | A | 1 | a0002c0002t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.837+7736G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039247 | ||||||
| chr10:49039484
|
C | T | 10 | a0002c0002t0003g0109a0002c0002t0003g0158a0002c0002t0003g0159others(7): Show | 10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+7499G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039484 | ||||||
| chr10:49039728
|
G | C | 1 | a0001c0004t0007g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+7255C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039728 | ||||||
| chr10:49039995
|
G | A | 1 | a0001c0001t0041g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.837+6988C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49039995 | ||||||
| chr10:49040182
|
C | T | 10 | a0002c0002t0003g0109a0002c0002t0003g0158a0002c0002t0003g0159others(7): Show | 10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+6801G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040182 | ||||||
| chr10:49040444
|
G | A | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.837+6539C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040444 | ||||||
| chr10:49040495
|
G | A | 11 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0011g0188others(8): Show | 11 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+6488C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040495 | ||||||
| chr10:49040497
|
G | A | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+6486C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040497 | ||||||
| chr10:49040539
|
G | A | 9 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.837+6444C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040539 | ||||||
| chr10:49040606
|
CCTA | C | 7 | a0001c0001t0020g0245a0001c0004t0007g0016a0001c0004t0007g0017others(4): Show | 8 | HG00639.hp2 HG02630.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.837+6374_837+6376d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040606 | ||||||
| chr10:49040741
|
C | T | 3 | a0001c0001t0022g0045a0001c0001t0022g0047a0001c0001t0023g0046 | 3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.837+6242G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040741 | ||||||
| chr10:49040777
|
C | T | 1 | a0001c0001t0029g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.837+6206G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040777 | ||||||
| chr10:49040833
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(106): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+6150G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040833 | ||||||
| chr10:49040879
|
G | A | 31 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(28): Show | 33 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.837+6104C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040879 | ||||||
| chr10:49040927
|
C | T | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+6056G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040927 | ||||||
| chr10:49040981
|
T | C | 49 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(46): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.837+6002A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49040981 | ||||||
| chr10:49041033
|
C | A | 49 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(46): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.837+5950G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041033 | ||||||
| chr10:49041191
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.837+5792C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041191 | ||||||
| chr10:49041464
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(106): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+5519A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041464 | ||||||
| chr10:49041641
|
G | T | 1 | a0001c0004t0007g0056 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.837+5342C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041641 | ||||||
| chr10:49041950
|
T | C | 3 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0122 | 3 | HG02056.hp1 NA18612.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.837+5033A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041950 | ||||||
| chr10:49041951
|
G | A | 10 | a0002c0002t0003g0109a0002c0002t0003g0158a0002c0002t0003g0159others(7): Show | 10 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+5032C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49041951 | ||||||
| chr10:49042559
|
G | T | 70 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(67): Show | 74 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.837+4424C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042559 | ||||||
| chr10:49042679
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.837+4304G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042679 | ||||||
| chr10:49042687
|
A | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(146): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.837+4296T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042687 | ||||||
| chr10:49042700
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.837+4283A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042700 | ||||||
| chr10:49042721
|
G | A | 1 | a0002c0002t0027g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.837+4262C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042721 | ||||||
| chr10:49042855
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.837+4128C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042855 | ||||||
| chr10:49042918
|
G | A | 2 | a0001c0001t0038g0198a0006c0011t0046g0264 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.837+4065C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042918 | ||||||
| chr10:49042918
|
G | C | 2 | a0002c0002t0001g0147a0002c0002t0001g0148 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.837+4065C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49042918 | ||||||
| chr10:49043048
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(106): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.837+3935T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043048 | ||||||
| chr10:49043056
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(146): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.837+3927A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043056 | ||||||
| chr10:49043445
|
T | C | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.837+3538A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043445 | ||||||
| chr10:49043584
|
T | G | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.837+3399A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043584 | ||||||
| chr10:49043620
|
A | G | 4 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0024g0185others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+3363T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043620 | ||||||
| chr10:49043622
|
A | G | 2 | a0001c0001t0038g0198a0006c0011t0046g0264 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.837+3361T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043622 | ||||||
| chr10:49043721
|
A | G | 1 | a0001c0001t0029g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.837+3262T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043721 | ||||||
| chr10:49043851
|
C | T | 1 | a0001c0001t0008g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.837+3132G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043851 | ||||||
| chr10:49043966
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.837+3017A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49043966 | ||||||
| chr10:49044018
|
G | A | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+2965C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044018 | ||||||
| chr10:49044090
|
C | T | 1 | a0001c0001t0009g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.837+2893G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044090 | ||||||
| chr10:49044119
|
T | G | 2 | a0001c0001t0008g0193a0001c0001t0048g0192 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.837+2864A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044119 | ||||||
| chr10:49044213
|
C | T | 22 | a0001c0001t0003g0011a0001c0001t0003g0251a0001c0001t0003g0252others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.837+2770G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044213 | ||||||
| chr10:49044395
|
G | A | 1 | a0002c0002t0003g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.837+2588C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044395 | ||||||
| chr10:49044409
|
AAGAG | A | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837+2570_837+2573d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044409 | ||||||
| chr10:49044431
|
AAAG | A | 6 | a0001c0001t0001g0034a0001c0001t0003g0036a0001c0001t0022g0045others(3): Show | 6 | HG02056.hp2 HG02083.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+2549_837+2551d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044431 | ||||||
| chr10:49044448
|
GAGAA | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+2531_837+2534d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044448 | ||||||
| chr10:49044526
|
GA | G | 34 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(31): Show | 35 | HG00099.hp1 HG00558.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.837+2456delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044526 | ||||||
| chr10:49044583
|
A | AAAG | 44 | a0001c0001t0002g0182a0001c0001t0003g0011a0001c0001t0003g0250others(41): Show | 46 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.837+2399_837+2400i others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044583 | ||||||
| chr10:49044740
|
C | T | 39 | a0001c0001t0002g0182a0001c0001t0003g0011a0001c0001t0003g0250others(36): Show | 41 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.837+2243G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044740 | ||||||
| chr10:49044813
|
G | A | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.837+2170C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044813 | ||||||
| chr10:49044891
|
G | A | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.837+2092C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044891 | ||||||
| chr10:49044956
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.837+2027G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044956 | ||||||
| chr10:49044977
|
T | C | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.837+2006A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044977 | ||||||
| chr10:49044983
|
T | C | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.837+2000A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49044983 | ||||||
| chr10:49045142
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(123): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+1841G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045142 | ||||||
| chr10:49045157
|
A | G | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.837+1826T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045157 | ||||||
| chr10:49045158
|
T | C | 23 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(20): Show | 23 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.837+1825A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045158 | ||||||
| chr10:49045202
|
T | TTC | 122 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0024others(119): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.837+1779_837+1780d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045202 | ||||||
| chr10:49045202
|
T | TTCTC | 4 | a0001c0005t0001g0176a0002c0002t0001g0082a0002c0002t0001g0085others(1): Show | 4 | HG00423.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+1777_837+1780d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045202 | ||||||
| chr10:49045415
|
G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01192.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+1568C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045415 | ||||||
| chr10:49045623
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(249): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.837+1360G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045623 | ||||||
| chr10:49045666
|
C | T | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.837+1317G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045666 | ||||||
| chr10:49045794
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.837+1189G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045794 | ||||||
| chr10:49045845
|
A | T | 1 | a0002c0002t0003g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.837+1138T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045845 | ||||||
| chr10:49045849
|
C | T | 7 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0011g0188others(4): Show | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+1134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045849 | ||||||
| chr10:49045875
|
T | A | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.837+1108A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49045875 | ||||||
| chr10:49046051
|
G | A | 7 | a0002c0002t0001g0081a0002c0002t0006g0078a0002c0002t0006g0079others(4): Show | 7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.837+932C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046051 | ||||||
| chr10:49046118
|
A | C | 85 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(82): Show | 89 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.837+865T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046118 | ||||||
| chr10:49046221
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(123): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+762G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046221 | ||||||
| chr10:49046254
|
A | T | 1 | a0001c0008t0007g0020 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.837+729T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046254 | ||||||
| chr10:49046335
|
C | T | 8 | a0001c0001t0011g0183a0001c0001t0042g0014a0001c0004t0007g0016others(5): Show | 9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+648G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046335 | ||||||
| chr10:49046534
|
C | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(155): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.837+449G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046534 | ||||||
| chr10:49046602
|
A | T | 8 | a0001c0001t0011g0183a0001c0001t0042g0014a0001c0004t0007g0016others(5): Show | 9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+381T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046602 | ||||||
| chr10:49046605
|
C | T | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.837+378G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046605 | ||||||
| chr10:49046894
|
A | G | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+89T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 7/7 | chr10 | 49046894 | ||||||
| chr10:49047206
|
G | A | 1 | a0002c0002t0003g0166 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.776-162C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047206 | ||||||
| chr10:49047267
|
T | G | 1 | a0002c0002t0025g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-223A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047267 | ||||||
| chr10:49047273
|
TA | T | 5 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0009g0174others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.776-230delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047273 | ||||||
| chr10:49047523
|
T | G | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.776-479A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047523 | ||||||
| chr10:49047878
|
T | C | 3 | a0001c0001t0003g0257a0001c0001t0003g0259a0001c0001t0020g0256 | 3 | HG02258.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.775+600A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047878 | ||||||
| chr10:49047887
|
C | T | 2 | a0001c0001t0002g0244a0002c0002t0002g0155 | 2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.775+591G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047887 | ||||||
| chr10:49047893
|
T | A | 5 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0009g0174others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+585A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047893 | ||||||
| chr10:49047920
|
T | C | 4 | a0001c0001t0040g0173a0002c0002t0017g0070a0002c0002t0017g0071others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+558A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49047920 | ||||||
| chr10:49048025
|
G | A | 8 | a0001c0001t0011g0183a0001c0001t0042g0014a0001c0004t0007g0016others(5): Show | 9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+453C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048025 | ||||||
| chr10:49048067
|
T | C | 6 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0011g0188others(3): Show | 6 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+411A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048067 | ||||||
| chr10:49048189
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(203): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.775+289A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048189 | ||||||
| chr10:49048209
|
A | G | 3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.775+269T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048209 | ||||||
| chr10:49048220
|
C | T | 6 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+258G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048220 | ||||||
| chr10:49048385
|
T | G | 1 | a0001c0003t0004g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.775+93A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 6/7 | chr10 | 49048385 | ||||||
| chr10:49048642
|
G | GA | 6 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0009g0174others(3): Show | 6 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-59dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048642 | ||||||
| chr10:49048758
|
G | T | 1 | a0002c0002t0007g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.669-174C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048758 | ||||||
| chr10:49048833
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669-249A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048833 | ||||||
| chr10:49048870
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(123): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.669-286G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048870 | ||||||
| chr10:49048898
|
G | C | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-314C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49048898 | ||||||
| chr10:49049280
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(123): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.669-696C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049280 | ||||||
| chr10:49049304
|
A | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-720T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049304 | ||||||
| chr10:49049418
|
G | A | 8 | a0001c0001t0011g0183a0001c0001t0042g0014a0001c0004t0007g0016others(5): Show | 9 | HG00639.hp2 HG02723.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.669-834C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049418 | ||||||
| chr10:49049491
|
G | T | 1 | a0002c0002t0010g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.669-907C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049491 | ||||||
| chr10:49049685
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(124): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.669-1101G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049685 | ||||||
| chr10:49049755
|
CT | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(154): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.669-1172delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049755 | ||||||
| chr10:49049833
|
G | C | 1 | a0001c0004t0007g0056 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.669-1249C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49049833 | ||||||
| chr10:49050062
|
A | AG | 164 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.669-1479dupC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050062 | ||||||
| chr10:49050095
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-1511C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050095 | ||||||
| chr10:49050311
|
A | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-1727T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050311 | ||||||
| chr10:49050438
|
C | A | 1 | a0002c0002t0003g0144 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669-1854G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050438 | ||||||
| chr10:49050660
|
C | T | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-2076G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050660 | ||||||
| chr10:49050686
|
A | G | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.669-2102T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050686 | ||||||
| chr10:49050690
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.669-2106G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050690 | ||||||
| chr10:49050784
|
G | T | 2 | a0001c0005t0009g0174a0001c0005t0009g0175 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.669-2200C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050784 | ||||||
| chr10:49050947
|
T | C | 48 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.669-2363A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050947 | ||||||
| chr10:49050962
|
C | G | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-2378G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49050962 | ||||||
| chr10:49051023
|
G | T | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-2439C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051023 | ||||||
| chr10:49051325
|
C | A | 1 | a0002c0002t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.669-2741G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051325 | ||||||
| chr10:49051390
|
C | CT | 38 | a0001c0001t0002g0182a0001c0001t0003g0011a0001c0001t0003g0250others(35): Show | 39 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.669-2807dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051390 | ||||||
| chr10:49051390
|
CT | C | 46 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(43): Show | 46 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.669-2807delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051390 | ||||||
| chr10:49051665
|
G | A | 1 | a0002c0002t0025g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669-3081C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051665 | ||||||
| chr10:49051883
|
T | C | 1 | a0002c0002t0002g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.669-3299A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051883 | ||||||
| chr10:49051955
|
T | TTG | 165 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(162): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.669-3372_669-3371i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49051955 | ||||||
| chr10:49052043
|
G | A | 1 | a0001c0001t0008g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.669-3459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052043 | ||||||
| chr10:49052243
|
T | G | 17 | a0002c0002t0001g0260a0002c0002t0002g0096a0002c0002t0006g0057others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.669-3659A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052243 | ||||||
| chr10:49052268
|
A | G | 1 | a0001c0001t0047g0248 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.669-3684T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052268 | ||||||
| chr10:49052275
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(240): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.669-3691G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052275 | ||||||
| chr10:49052433
|
A | AT | 42 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(39): Show | 45 | HG00099.hp1 HG00423.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.669-3850dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | ||||||
| chr10:49052433
|
A | ATT | 116 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.669-3851_669-3850d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | ||||||
| chr10:49052433
|
A | ATTTT | 5 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-3853_669-3850d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | ||||||
| chr10:49052433
|
AT | A | 11 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0158others(8): Show | 11 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-3850delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052433 | ||||||
| chr10:49052542
|
A | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669-3958T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052542 | ||||||
| chr10:49052551
|
GA | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(240): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.669-3968delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052551 | ||||||
| chr10:49052558
|
A | C | 1 | a0001c0001t0002g0223 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.669-3974T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052558 | ||||||
| chr10:49052693
|
C | T | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.669-4109G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052693 | ||||||
| chr10:49052808
|
T | C | 1 | a0002c0002t0007g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.669-4224A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052808 | ||||||
| chr10:49052831
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.669-4247C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49052831 | ||||||
| chr10:49053090
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-4506C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053090 | ||||||
| chr10:49053199
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.669-4615C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053199 | ||||||
| chr10:49053380
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0009g0174others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-4796G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053380 | ||||||
| chr10:49053388
|
T | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669-4804A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053388 | ||||||
| chr10:49053482
|
C | T | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.669-4898G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053482 | ||||||
| chr10:49053558
|
G | A | 1 | a0001c0001t0008g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.669-4974C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053558 | ||||||
| chr10:49053562
|
G | C | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-4978C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053562 | ||||||
| chr10:49053629
|
A | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669-5045T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053629 | ||||||
| chr10:49053684
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.669-5100C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053684 | ||||||
| chr10:49053714
|
G | T | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-5130C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053714 | ||||||
| chr10:49053732
|
T | G | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-5148A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053732 | ||||||
| chr10:49053835
|
C | T | 24 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.669-5251G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053835 | ||||||
| chr10:49053884
|
G | A | 13 | a0001c0001t0025g0179a0002c0002t0002g0156a0002c0002t0002g0157others(10): Show | 13 | HG00558.hp1 HG03225.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.669-5300C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053884 | ||||||
| chr10:49053910
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0106a0002c0002t0001g0116others(1): Show | 6 | HG02027.hp2 NA18612.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-5326C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053910 | ||||||
| chr10:49053914
|
A | C | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.669-5330T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49053914 | ||||||
| chr10:49054065
|
C | A | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-5481G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054065 | ||||||
| chr10:49054099
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.669-5515A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054099 | ||||||
| chr10:49054193
|
C | T | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669-5609G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054193 | ||||||
| chr10:49054257
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.669-5673C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054257 | ||||||
| chr10:49054426
|
G | A | 2 | a0001c0001t0018g0169a0001c0001t0018g0170 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.669-5842C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054426 | ||||||
| chr10:49054561
|
A | G | 1 | a0002c0002t0001g0148 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669-5977T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054561 | ||||||
| chr10:49054643
|
G | C | 4 | a0002c0002t0001g0075a0002c0002t0013g0008a0002c0002t0013g0073others(1): Show | 5 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-6059C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054643 | ||||||
| chr10:49054907
|
T | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.669-6323A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054907 | ||||||
| chr10:49054938
|
AG | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(118): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.669-6355delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054938 | ||||||
| chr10:49054991
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.669-6407C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49054991 | ||||||
| chr10:49055033
|
T | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.669-6449A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055033 | ||||||
| chr10:49055049
|
G | C | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.669-6465C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055049 | ||||||
| chr10:49055085
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.669-6501A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055085 | ||||||
| chr10:49055156
|
A | G | 75 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0207others(72): Show | 76 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.669-6572T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055156 | ||||||
| chr10:49055168
|
G | A | 10 | a0001c0001t0001g0221a0001c0001t0001g0231a0001c0001t0002g0216others(7): Show | 10 | HG01952.hp2 HG01975.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.669-6584C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055168 | ||||||
| chr10:49055232
|
C | A | 3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.669-6648G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055232 | ||||||
| chr10:49055264
|
T | C | 1 | a0002c0002t0003g0144 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.669-6680A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055264 | ||||||
| chr10:49055278
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0009g0174others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-6694G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055278 | ||||||
| chr10:49055285
|
G | A | 1 | a0002c0002t0006g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.669-6701C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055285 | ||||||
| chr10:49055363
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(260): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.669-6779A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055363 | ||||||
| chr10:49055498
|
G | A | 54 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(51): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.669-6914C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055498 | ||||||
| chr10:49055569
|
C | G | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.669-6985G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055569 | ||||||
| chr10:49055831
|
G | A | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-7247C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055831 | ||||||
| chr10:49055871
|
A | G | 11 | a0001c0001t0011g0012a0001c0001t0011g0186a0001c0001t0011g0188others(8): Show | 11 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.669-7287T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055871 | ||||||
| chr10:49055928
|
G | A | 17 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0186others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-7344C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49055928 | ||||||
| chr10:49056002
|
C | T | 158 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(155): Show | 166 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.669-7418G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056002 | ||||||
| chr10:49056050
|
G | C | 17 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0186others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-7466C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056050 | ||||||
| chr10:49056159
|
C | G | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.669-7575G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056159 | ||||||
| chr10:49056203
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.669-7619T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056203 | ||||||
| chr10:49056350
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0028g0178 | 2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669-7766C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056350 | ||||||
| chr10:49056496
|
G | A | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-7912C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056496 | ||||||
| chr10:49056762
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.668+7941G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056762 | ||||||
| chr10:49056918
|
T | C | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.668+7785A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056918 | ||||||
| chr10:49056985
|
C | T | 23 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.668+7718G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056985 | ||||||
| chr10:49056986
|
G | A | 98 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+7717C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49056986 | ||||||
| chr10:49057000
|
G | A | 98 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+7703C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057000 | ||||||
| chr10:49057005
|
G | T | 3 | a0001c0001t0008g0193a0001c0001t0008g0196a0001c0001t0048g0192 | 3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.668+7698C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057005 | ||||||
| chr10:49057022
|
G | A | 1 | a0002c0002t0001g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.668+7681C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057022 | ||||||
| chr10:49057251
|
G | C | 1 | a0002c0002t0006g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.668+7452C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057251 | ||||||
| chr10:49057340
|
A | G | 1 | a0001c0001t0011g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.668+7363T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057340 | ||||||
| chr10:49057545
|
G | T | 17 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0186others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.668+7158C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057545 | ||||||
| chr10:49057547
|
C | T | 1 | a0002c0002t0003g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.668+7156G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057547 | ||||||
| chr10:49057670
|
G | T | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.668+7033C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057670 | ||||||
| chr10:49057864
|
A | C | 1 | a0002c0002t0025g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668+6839T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49057864 | ||||||
| chr10:49058154
|
C | T | 2 | a0001c0001t0011g0183a0001c0001t0042g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+6549G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058154 | ||||||
| chr10:49058244
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(118): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.668+6459C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058244 | ||||||
| chr10:49058354
|
A | G | 1 | a0001c0003t0004g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668+6349T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058354 | ||||||
| chr10:49058589
|
AG | A | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+6113delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058589 | ||||||
| chr10:49058885
|
G | T | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.668+5818C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058885 | ||||||
| chr10:49058905
|
T | C | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+5798A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058905 | ||||||
| chr10:49058937
|
G | T | 46 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(43): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.668+5766C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49058937 | ||||||
| chr10:49059010
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0028g0178 | 2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.668+5693G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059010 | ||||||
| chr10:49059046
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.668+5657T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059046 | ||||||
| chr10:49059053
|
C | A | 1 | a0002c0002t0006g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.668+5650G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059053 | ||||||
| chr10:49059448
|
A | G | 124 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(121): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.668+5255T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059448 | ||||||
| chr10:49059526
|
C | T | 1 | a0002c0002t0006g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.668+5177G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059526 | ||||||
| chr10:49059597
|
A | C | 6 | a0002c0002t0001g0075a0002c0002t0001g0084a0002c0002t0013g0008others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+5106T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059597 | ||||||
| chr10:49059608
|
C | G | 1 | a0002c0002t0007g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.668+5095G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059608 | ||||||
| chr10:49059734
|
T | C | 20 | a0001c0001t0019g0180a0001c0001t0019g0181a0002c0002t0001g0260others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.668+4969A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059734 | ||||||
| chr10:49059742
|
G | A | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668+4961C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059742 | ||||||
| chr10:49059851
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0003g0217a0002c0002t0002g0125 | 3 | HG00558.hp2 HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.668+4852C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49059851 | ||||||
| chr10:49060230
|
C | T | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.668+4473G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060230 | ||||||
| chr10:49060231
|
G | A | 7 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(4): Show | 8 | HG00639.hp2 HG03041.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+4472C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060231 | ||||||
| chr10:49060387
|
T | C | 1 | a0001c0001t0002g0235 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.668+4316A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060387 | ||||||
| chr10:49060397
|
A | C | 48 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.668+4306T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060397 | ||||||
| chr10:49060535
|
T | G | 1 | a0001c0004t0007g0019 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.668+4168A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060535 | ||||||
| chr10:49060554
|
T | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+4149A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060554 | ||||||
| chr10:49060572
|
G | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+4131C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060572 | ||||||
| chr10:49060655
|
T | G | 1 | a0002c0002t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.668+4048A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060655 | ||||||
| chr10:49060718
|
T | C | 157 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(154): Show | 165 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.668+3985A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060718 | ||||||
| chr10:49060878
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+3825T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060878 | ||||||
| chr10:49060893
|
T | G | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.668+3810A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49060893 | ||||||
| chr10:49061052
|
A | G | 1 | a0001c0001t0005g0049 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.668+3651T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061052 | ||||||
| chr10:49061077
|
T | C | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.668+3626A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061077 | ||||||
| chr10:49061162
|
A | T | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.668+3541T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061162 | ||||||
| chr10:49061205
|
T | C | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+3498A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061205 | ||||||
| chr10:49061238
|
G | A | 3 | a0001c0003t0004g0211a0001c0003t0004g0212a0001c0003t0004g0213 | 3 | HG02109.hp1 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.668+3465C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061238 | ||||||
| chr10:49061442
|
T | G | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.668+3261A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061442 | ||||||
| chr10:49061496
|
C | T | 179 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(176): Show | 188 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.668+3207G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061496 | ||||||
| chr10:49061556
|
T | G | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.668+3147A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061556 | ||||||
| chr10:49061572
|
G | A | 1 | a0002c0002t0006g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.668+3131C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061572 | ||||||
| chr10:49061601
|
C | A | 7 | a0001c0001t0038g0198a0001c0004t0007g0016a0001c0004t0007g0017others(4): Show | 8 | HG00639.hp2 HG01243.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.668+3102G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061601 | ||||||
| chr10:49061639
|
G | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(119): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+3064C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061639 | ||||||
| chr10:49061668
|
A | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.668+3035T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061668 | ||||||
| chr10:49061907
|
A | G | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.668+2796T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49061907 | ||||||
| chr10:49062177
|
C | T | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.668+2526G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062177 | ||||||
| chr10:49062312
|
ATT | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(119): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+2389_668+2390d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062312 | ||||||
| chr10:49062321
|
T | C | 1 | a0005c0009t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.668+2382A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062321 | ||||||
| chr10:49062332
|
T | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(119): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+2371A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062332 | ||||||
| chr10:49062335
|
ATTTTAGT others(87): Show |
A | 2 | a0002c0002t0006g0057a0002c0002t0006g0058 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.668+2274_668+2367d others(96): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062335 | ||||||
| chr10:49062418
|
T | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(119): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.668+2285A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062418 | ||||||
| chr10:49062777
|
T | C | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+1926A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062777 | ||||||
| chr10:49062965
|
T | C | 1 | a0002c0002t0006g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.668+1738A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49062965 | ||||||
| chr10:49063025
|
C | CTT | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.668+1676_668+1677d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063025 | ||||||
| chr10:49063025
|
CT | C | 41 | a0001c0001t0002g0216a0001c0001t0003g0018a0001c0001t0003g0207others(38): Show | 41 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.668+1677delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063025 | ||||||
| chr10:49063190
|
T | A | 158 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(155): Show | 166 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.668+1513A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063190 | ||||||
| chr10:49063364
|
T | G | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+1339A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063364 | ||||||
| chr10:49063627
|
G | C | 3 | a0001c0005t0009g0174a0001c0005t0009g0175a0001c0005t0009g0177 | 3 | HG02572.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.668+1076C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063627 | ||||||
| chr10:49063755
|
G | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.668+948C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063755 | ||||||
| chr10:49063812
|
G | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.668+891C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063812 | ||||||
| chr10:49063947
|
G | A | 2 | a0002c0002t0001g0152a0002c0002t0012g0010 | 3 | HG00438.hp2 NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.668+756C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49063947 | ||||||
| chr10:49064037
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.668+666G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064037 | ||||||
| chr10:49064174
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.668+529C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064174 | ||||||
| chr10:49064261
|
CT | C | 3 | a0001c0001t0005g0061a0001c0001t0005g0062a0001c0001t0005g0063 | 3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.668+441delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064261 | ||||||
| chr10:49064336
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.668+367G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064336 | ||||||
| chr10:49064427
|
T | C | 99 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(96): Show | 103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.668+276A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 5/7 | chr10 | 49064427 | ||||||
| chr10:49065142
|
C | A | 3 | a0001c0005t0001g0176a0002c0002t0001g0082a0002c0002t0001g0085 | 3 | HG02257.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.635-406G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065142 | ||||||
| chr10:49065204
|
C | T | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.635-468G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065204 | ||||||
| chr10:49065356
|
G | T | 1 | a0001c0001t0022g0047 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.635-620C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065356 | ||||||
| chr10:49065747
|
T | C | 7 | a0002c0002t0001g0081a0002c0002t0006g0078a0002c0002t0006g0079others(4): Show | 7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-1011A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065747 | ||||||
| chr10:49065759
|
G | A | 1 | a0002c0002t0013g0074 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.635-1023C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49065759 | ||||||
| chr10:49066196
|
A | G | 158 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(155): Show | 166 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.635-1460T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066196 | ||||||
| chr10:49066241
|
T | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.635-1505A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066241 | ||||||
| chr10:49066281
|
C | G | 1 | a0001c0003t0004g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.635-1545G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066281 | ||||||
| chr10:49066553
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 15 | HG01192.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-1817A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066553 | ||||||
| chr10:49066628
|
T | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.635-1892A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066628 | ||||||
| chr10:49066683
|
C | T | 99 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(96): Show | 103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.635-1947G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066683 | ||||||
| chr10:49066734
|
A | T | 1 | a0002c0002t0002g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.635-1998T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49066734 | ||||||
| chr10:49067014
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.635-2278T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067014 | ||||||
| chr10:49067049
|
C | A | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.635-2313G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067049 | ||||||
| chr10:49067115
|
C | A | 1 | a0001c0001t0020g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.635-2379G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067115 | ||||||
| chr10:49067204
|
ATGAT | A | 50 | a0001c0001t0003g0018a0001c0001t0003g0207a0001c0001t0011g0012others(47): Show | 50 | HG00558.hp1 HG00642.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.635-2472_635-2469d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067204 | ||||||
| chr10:49067208
|
T | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.635-2472A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067208 | ||||||
| chr10:49067250
|
C | G | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.635-2514G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067250 | ||||||
| chr10:49067317
|
T | C | 10 | a0001c0003t0004g0200a0001c0003t0004g0202a0001c0003t0004g0204others(7): Show | 10 | HG01109.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.635-2581A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067317 | ||||||
| chr10:49067487
|
T | C | 27 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(24): Show | 28 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.635-2751A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067487 | ||||||
| chr10:49067518
|
C | G | 48 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.635-2782G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067518 | ||||||
| chr10:49067669
|
T | C | 1 | a0002c0002t0012g0067 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.635-2933A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067669 | ||||||
| chr10:49067936
|
C | T | 17 | a0002c0002t0001g0260a0002c0002t0002g0096a0002c0002t0006g0057others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-3200G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49067936 | ||||||
| chr10:49068017
|
T | C | 3 | a0001c0001t0005g0061a0001c0001t0005g0062a0001c0001t0005g0063 | 3 | HG00423.hp2 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.635-3281A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068017 | ||||||
| chr10:49068049
|
T | C | 1 | a0001c0001t0011g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.635-3313A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068049 | ||||||
| chr10:49068066
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0028g0178 | 2 | HG01106.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.635-3330T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068066 | ||||||
| chr10:49068252
|
A | G | 137 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(134): Show | 143 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.635-3516T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068252 | ||||||
| chr10:49068325
|
C | T | 1 | a0001c0003t0044g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.635-3589G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068325 | ||||||
| chr10:49068407
|
C | T | 1 | a0001c0003t0004g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.635-3671G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068407 | ||||||
| chr10:49068462
|
T | G | 1 | a0001c0001t0009g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.635-3726A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068462 | ||||||
| chr10:49068528
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.635-3792C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068528 | ||||||
| chr10:49068690
|
G | A | 17 | a0002c0002t0001g0260a0002c0002t0002g0096a0002c0002t0006g0057others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-3954C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068690 | ||||||
| chr10:49068780
|
C | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.635-4044G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068780 | ||||||
| chr10:49068879
|
C | T | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.635-4143G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068879 | ||||||
| chr10:49068924
|
A | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.635-4188T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49068924 | ||||||
| chr10:49069530
|
G | T | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.635-4794C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069530 | ||||||
| chr10:49069540
|
C | T | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.635-4804G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069540 | ||||||
| chr10:49069548
|
G | C | 1 | a0001c0001t0011g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.635-4812C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069548 | ||||||
| chr10:49069630
|
A | G | 1 | a0002c0002t0001g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.635-4894T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069630 | ||||||
| chr10:49069653
|
G | C | 121 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(118): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.635-4917C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069653 | ||||||
| chr10:49069684
|
A | G | 8 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(5): Show | 8 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-4948T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069684 | ||||||
| chr10:49069870
|
C | T | 1 | a0002c0002t0001g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-5134G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069870 | ||||||
| chr10:49069970
|
CGGCCGGG others(310): Show |
C | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.635-5551_635-5235d others(2): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49069970 | ||||||
| chr10:49070027
|
C | T | 1 | a0002c0002t0001g0149 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.635-5291G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070027 | ||||||
| chr10:49070049
|
G | A | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5313C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070049 | ||||||
| chr10:49070068
|
C | T | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5332G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070068 | ||||||
| chr10:49070105
|
C | T | 58 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 62 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.635-5369G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070105 | ||||||
| chr10:49070126
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.635-5390C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070126 | ||||||
| chr10:49070178
|
G | A | 1 | a0001c0004t0007g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.635-5442C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070178 | ||||||
| chr10:49070252
|
C | CA | 15 | a0001c0001t0001g0262a0001c0004t0007g0019a0002c0002t0001g0128others(12): Show | 15 | HG00323.hp1 HG01106.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-5517dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAA | 8 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-5518_635-5517d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAAAA | 6 | a0001c0001t0005g0006a0002c0002t0006g0078a0002c0002t0006g0079others(3): Show | 7 | HG02559.hp1 HG02922.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5520_635-5517d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAAAAA | 7 | a0001c0001t0002g0182a0001c0001t0018g0170a0001c0001t0018g0171others(4): Show | 7 | HG01071.hp1 HG02080.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-5521_635-5517d others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAAAAAAA others(4): Show |
10 | a0001c0001t0005g0007a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 11 | NA18941.hp2 NA18948.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-5527_635-5517d others(13): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | NA18947.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.635-5528_635-5517d others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0005g0062 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.635-5529_635-5517d others(15): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070252
|
CAA | C | 6 | a0002c0002t0001g0075a0002c0002t0001g0084a0002c0002t0013g0008others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-5518_635-5517d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070252 | ||||||
| chr10:49070287
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(134): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.635-5551C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070287 | ||||||
| chr10:49070346
|
G | A | 2 | a0001c0001t0040g0173a0006c0011t0046g0264 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.635-5610C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070346 | ||||||
| chr10:49070412
|
TA | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(118): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.635-5677delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070412 | ||||||
| chr10:49070489
|
T | C | 7 | a0002c0002t0001g0081a0002c0002t0006g0078a0002c0002t0006g0079others(4): Show | 7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-5753A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070489 | ||||||
| chr10:49070581
|
C | T | 1 | a0002c0002t0014g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.635-5845G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070581 | ||||||
| chr10:49070631
|
G | C | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.635-5895C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070631 | ||||||
| chr10:49070803
|
C | T | 1 | a0002c0002t0016g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.635-6067G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49070803 | ||||||
| chr10:49071343
|
G | A | 1 | a0001c0001t0047g0248 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634+5876C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071343 | ||||||
| chr10:49071458
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.634+5761T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071458 | ||||||
| chr10:49071682
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.634+5537G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071682 | ||||||
| chr10:49071750
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+5469A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071750 | ||||||
| chr10:49071910
|
C | G | 1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+5309G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071910 | ||||||
| chr10:49071994
|
C | T | 14 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0200others(11): Show | 14 | HG01109.hp1 HG01981.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+5225G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49071994 | ||||||
| chr10:49072044
|
A | G | 1 | a0002c0002t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.634+5175T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072044 | ||||||
| chr10:49072193
|
C | T | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.634+5026G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072193 | ||||||
| chr10:49072211
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634+5008C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072211 | ||||||
| chr10:49072432
|
G | A | 1 | a0001c0001t0005g0049 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.634+4787C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072432 | ||||||
| chr10:49072598
|
G | A | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+4621C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072598 | ||||||
| chr10:49072747
|
C | T | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.634+4472G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072747 | ||||||
| chr10:49072882
|
C | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+4337G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072882 | ||||||
| chr10:49072883
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+4336T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072883 | ||||||
| chr10:49072989
|
C | A | 125 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(122): Show | 130 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.634+4230G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49072989 | ||||||
| chr10:49073044
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+4175C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073044 | ||||||
| chr10:49073069
|
G | A | 20 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(17): Show | 20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+4150C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073069 | ||||||
| chr10:49073180
|
G | T | 6 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+4039C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073180 | ||||||
| chr10:49073311
|
C | T | 99 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(96): Show | 103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.634+3908G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073311 | ||||||
| chr10:49073346
|
G | A | 1 | a0001c0005t0009g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.634+3873C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073346 | ||||||
| chr10:49073394
|
C | A | 1 | a0002c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.634+3825G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073394 | ||||||
| chr10:49073455
|
C | T | 4 | a0001c0001t0009g0027a0001c0001t0009g0029a0001c0001t0009g0030others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+3764G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073455 | ||||||
| chr10:49073602
|
C | G | 7 | a0002c0002t0001g0081a0002c0002t0006g0078a0002c0002t0006g0079others(4): Show | 7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+3617G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073602 | ||||||
| chr10:49073665
|
C | T | 1 | a0001c0003t0004g0215 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.634+3554G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073665 | ||||||
| chr10:49073835
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+3384T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073835 | ||||||
| chr10:49073846
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+3373G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073846 | ||||||
| chr10:49073851
|
A | G | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.634+3368T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073851 | ||||||
| chr10:49073900
|
C | T | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+3319G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073900 | ||||||
| chr10:49073946
|
T | C | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.634+3273A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49073946 | ||||||
| chr10:49074184
|
A | G | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.634+3035T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074184 | ||||||
| chr10:49074331
|
G | C | 3 | a0001c0001t0022g0045a0001c0001t0022g0047a0001c0001t0023g0046 | 3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.634+2888C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074331 | ||||||
| chr10:49074478
|
C | T | 1 | a0002c0002t0001g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.634+2741G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074478 | ||||||
| chr10:49074497
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.634+2722C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074497 | ||||||
| chr10:49074503
|
G | A | 20 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(17): Show | 20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+2716C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074503 | ||||||
| chr10:49074727
|
T | G | 18 | a0002c0002t0001g0260a0002c0002t0002g0096a0002c0002t0006g0057others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.634+2492A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074727 | ||||||
| chr10:49074828
|
G | A | 13 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(10): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+2391C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49074828 | ||||||
| chr10:49075047
|
G | A | 10 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(7): Show | 10 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+2172C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075047 | ||||||
| chr10:49075109
|
A | G | 106 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(103): Show | 107 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.634+2110T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075109 | ||||||
| chr10:49075199
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+2020A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075199 | ||||||
| chr10:49075249
|
T | C | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.634+1970A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075249 | ||||||
| chr10:49075282
|
A | T | 2 | a0001c0001t0020g0245a0001c0001t0041g0247 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.634+1937T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075282 | ||||||
| chr10:49075378
|
G | A | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+1841C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075378 | ||||||
| chr10:49075480
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.634+1739G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075480 | ||||||
| chr10:49075494
|
T | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.634+1725A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075494 | ||||||
| chr10:49075619
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.634+1600G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075619 | ||||||
| chr10:49075721
|
T | C | 1 | a0002c0002t0001g0149 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.634+1498A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075721 | ||||||
| chr10:49075771
|
T | C | 1 | a0001c0001t0010g0232 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.634+1448A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075771 | ||||||
| chr10:49075851
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.634+1368C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075851 | ||||||
| chr10:49075862
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(120): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.634+1357T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49075862 | ||||||
| chr10:49076109
|
C | T | 99 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(96): Show | 103 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.634+1110G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076109 | ||||||
| chr10:49076426
|
G | A | 1 | a0002c0002t0049g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+793C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076426 | ||||||
| chr10:49076428
|
C | CGGAAGTA others(36): Show |
1 | a0002c0002t0049g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+790_634+791ins others(43): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076428 | ||||||
| chr10:49076430
|
C | A | 1 | a0002c0002t0049g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+789G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076430 | ||||||
| chr10:49076458
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.634+761C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076458 | ||||||
| chr10:49076600
|
A | C | 127 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(124): Show | 132 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.634+619T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076600 | ||||||
| chr10:49076615
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.634+604T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076615 | ||||||
| chr10:49076651
|
T | C | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+568A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076651 | ||||||
| chr10:49076897
|
C | A | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+322G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49076897 | ||||||
| chr10:49077001
|
C | T | 24 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(21): Show | 25 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.634+218G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077001 | ||||||
| chr10:49077002
|
G | A | 1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+217C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077002 | ||||||
| chr10:49077039
|
A | C | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.634+180T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077039 | ||||||
| chr10:49077090
|
A | G | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634+129T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 4/7 | chr10 | 49077090 | ||||||
| chr10:49077432
|
A | T | 1 | a0001c0001t0009g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.527-106T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077432 | ||||||
| chr10:49077597
|
T | G | 1 | a0002c0002t0025g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.527-271A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077597 | ||||||
| chr10:49077614
|
G | A | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.527-288C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077614 | ||||||
| chr10:49077712
|
G | GA | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-387dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077712 | ||||||
| chr10:49077832
|
A | T | 1 | a0001c0004t0007g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.527-506T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077832 | ||||||
| chr10:49077861
|
A | G | 87 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(84): Show | 92 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.527-535T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077861 | ||||||
| chr10:49077993
|
GA | G | 104 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(101): Show | 111 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.527-668delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49077993 | ||||||
| chr10:49078477
|
GAC | G | 23 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.527-1153_527-1152d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078477 | ||||||
| chr10:49078497
|
T | A | 1 | a0001c0001t0002g0226 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.527-1171A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078497 | ||||||
| chr10:49078500
|
A | C | 1 | a0001c0001t0009g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.527-1174T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078500 | ||||||
| chr10:49078523
|
G | GA | 29 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(26): Show | 31 | HG00423.hp2 HG00558.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.527-1198dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | ||||||
| chr10:49078523
|
G | GAA | 93 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(90): Show | 98 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.527-1199_527-1198d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | ||||||
| chr10:49078523
|
GA | G | 13 | a0001c0001t0001g0023a0001c0001t0009g0027a0001c0001t0009g0028others(10): Show | 14 | HG00639.hp2 HG01884.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.527-1198delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078523 | ||||||
| chr10:49078575
|
T | C | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.527-1249A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078575 | ||||||
| chr10:49078580
|
G | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-1254C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078580 | ||||||
| chr10:49078826
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.527-1500A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078826 | ||||||
| chr10:49078849
|
A | AT | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.527-1524dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078849 | ||||||
| chr10:49078984
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.527-1658C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49078984 | ||||||
| chr10:49079109
|
G | A | 3 | a0002c0002t0001g0107a0002c0002t0001g0128a0002c0002t0012g0127 | 3 | HG01106.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.527-1783C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079109 | ||||||
| chr10:49079183
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.527-1857C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079183 | ||||||
| chr10:49079437
|
C | T | 1 | a0002c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.527-2111G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079437 | ||||||
| chr10:49079502
|
A | G | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.527-2176T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079502 | ||||||
| chr10:49079527
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.527-2201T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079527 | ||||||
| chr10:49079642
|
A | T | 2 | a0001c0001t0020g0256a0001c0003t0004g0255 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.527-2316T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079642 | ||||||
| chr10:49079753
|
G | A | 134 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(131): Show | 140 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.527-2427C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079753 | ||||||
| chr10:49079808
|
GA | G | 85 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(82): Show | 90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-2483delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079808 | ||||||
| chr10:49079822
|
C | T | 85 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(82): Show | 90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-2496G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079822 | ||||||
| chr10:49079845
|
AACT | A | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-2522_527-2520d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079845 | ||||||
| chr10:49079924
|
C | CT | 85 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(82): Show | 90 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.527-2599dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49079924 | ||||||
| chr10:49080216
|
G | A | 28 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(25): Show | 29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.527-2890C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080216 | ||||||
| chr10:49080273
|
A | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-2947T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080273 | ||||||
| chr10:49080358
|
C | T | 7 | a0002c0002t0001g0081a0002c0002t0006g0078a0002c0002t0006g0079others(4): Show | 7 | HG02080.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-3032G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080358 | ||||||
| chr10:49080571
|
T | A | 1 | a0002c0002t0001g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.527-3245A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080571 | ||||||
| chr10:49080754
|
C | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-3428G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080754 | ||||||
| chr10:49080778
|
G | T | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-3452C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080778 | ||||||
| chr10:49080886
|
G | T | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.527-3560C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49080886 | ||||||
| chr10:49081083
|
A | G | 16 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0183others(13): Show | 16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.527-3757T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081083 | ||||||
| chr10:49081180
|
C | A | 1 | a0004c0007t0003g0154 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.527-3854G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081180 | ||||||
| chr10:49081551
|
C | T | 2 | a0002c0002t0003g0110a0002c0002t0003g0144 | 2 | NA19070.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.527-4225G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081551 | ||||||
| chr10:49081583
|
C | G | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.527-4257G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081583 | ||||||
| chr10:49081597
|
G | T | 1 | a0001c0001t0002g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527-4271C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081597 | ||||||
| chr10:49081616
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.527-4290C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081616 | ||||||
| chr10:49081940
|
C | T | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+4015G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49081940 | ||||||
| chr10:49082131
|
G | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+3824C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082131 | ||||||
| chr10:49082379
|
T | C | 1 | a0002c0002t0001g0119 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.526+3576A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082379 | ||||||
| chr10:49082400
|
A | T | 6 | a0001c0001t0003g0018a0001c0001t0028g0178a0001c0005t0001g0176others(3): Show | 6 | HG01106.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+3555T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082400 | ||||||
| chr10:49082437
|
A | G | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3518T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082437 | ||||||
| chr10:49082451
|
G | A | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3504C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082451 | ||||||
| chr10:49082460
|
T | C | 48 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.526+3495A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082460 | ||||||
| chr10:49082473
|
T | G | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3482A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082473 | ||||||
| chr10:49082497
|
T | C | 5 | a0001c0003t0004g0211a0001c0003t0004g0212a0001c0003t0004g0213others(2): Show | 5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3458A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082497 | ||||||
| chr10:49082511
|
C | T | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526+3444G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082511 | ||||||
| chr10:49082547
|
T | C | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3408A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082547 | ||||||
| chr10:49082603
|
A | T | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3352T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082603 | ||||||
| chr10:49082631
|
T | C | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+3324A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082631 | ||||||
| chr10:49082674
|
A | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+3281T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082674 | ||||||
| chr10:49082690
|
G | GA | 5 | a0001c0001t0039g0167a0001c0001t0042g0014a0001c0003t0044g0201others(2): Show | 5 | HG01981.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3264dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082690 | ||||||
| chr10:49082690
|
G | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.526+3265C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082690 | ||||||
| chr10:49082921
|
T | A | 2 | a0001c0001t0021g0241a0001c0001t0021g0242 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.526+3034A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49082921 | ||||||
| chr10:49083169
|
T | A | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526+2786A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083169 | ||||||
| chr10:49083355
|
C | G | 91 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(88): Show | 96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.526+2600G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083355 | ||||||
| chr10:49083521
|
G | A | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526+2434C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083521 | ||||||
| chr10:49083806
|
G | A | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+2149C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083806 | ||||||
| chr10:49083845
|
T | C | 1 | a0002c0002t0002g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.526+2110A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083845 | ||||||
| chr10:49083888
|
C | G | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.526+2067G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083888 | ||||||
| chr10:49083917
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.526+2038G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49083917 | ||||||
| chr10:49084169
|
A | G | 1 | a0002c0002t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.526+1786T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084169 | ||||||
| chr10:49084401
|
C | T | 28 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(25): Show | 29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+1554G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084401 | ||||||
| chr10:49084438
|
A | C | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.526+1517T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084438 | ||||||
| chr10:49084765
|
G | C | 1 | a0002c0002t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.526+1190C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084765 | ||||||
| chr10:49084780
|
G | A | 1 | a0002c0002t0032g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+1175C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084780 | ||||||
| chr10:49084965
|
C | A | 1 | a0002c0002t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.526+990G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49084965 | ||||||
| chr10:49085014
|
A | C | 86 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(83): Show | 91 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.526+941T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085014 | ||||||
| chr10:49085058
|
T | A | 1 | a0002c0002t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.526+897A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085058 | ||||||
| chr10:49085112
|
G | T | 1 | a0002c0002t0003g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.526+843C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085112 | ||||||
| chr10:49085213
|
C | T | 134 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(131): Show | 140 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.526+742G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085213 | ||||||
| chr10:49085269
|
C | T | 4 | a0001c0005t0001g0176a0001c0005t0009g0174a0001c0005t0009g0175others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+686G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085269 | ||||||
| chr10:49085411
|
A | G | 155 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(152): Show | 163 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.526+544T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085411 | ||||||
| chr10:49085522
|
G | A | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.526+433C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085522 | ||||||
| chr10:49085855
|
G | A | 1 | a0002c0002t0030g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.526+100C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085855 | ||||||
| chr10:49085891
|
T | A | 28 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(25): Show | 29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.526+64A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085891 | ||||||
| chr10:49085909
|
A | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.526+46T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085909 | ||||||
| chr10:49085928
|
TA | T | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+26delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 3/7 | chr10 | 49085928 | ||||||
| chr10:49086217
|
C | T | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-194G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086217 | ||||||
| chr10:49086218
|
A | G | 116 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(113): Show | 122 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.458-195T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086218 | ||||||
| chr10:49086387
|
C | T | 16 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0183others(13): Show | 16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-364G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086387 | ||||||
| chr10:49086398
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-375A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086398 | ||||||
| chr10:49086444
|
T | C | 1 | a0001c0001t0036g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458-421A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086444 | ||||||
| chr10:49086625
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(197): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.458-602C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086625 | ||||||
| chr10:49086630
|
C | T | 31 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(28): Show | 31 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.458-607G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086630 | ||||||
| chr10:49086683
|
C | T | 33 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0039g0167others(30): Show | 33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-660G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086683 | ||||||
| chr10:49086860
|
T | C | 33 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0039g0167others(30): Show | 33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-837A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086860 | ||||||
| chr10:49086966
|
A | C | 156 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(153): Show | 164 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.458-943T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49086966 | ||||||
| chr10:49087009
|
C | T | 28 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(25): Show | 29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-986G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087009 | ||||||
| chr10:49087347
|
C | T | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-1324G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087347 | ||||||
| chr10:49087412
|
T | A | 1 | a0002c0002t0025g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.458-1389A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087412 | ||||||
| chr10:49087786
|
G | A | 33 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0039g0167others(30): Show | 33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-1763C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087786 | ||||||
| chr10:49087881
|
C | T | 16 | a0001c0001t0003g0018a0001c0001t0011g0012a0001c0001t0011g0183others(13): Show | 16 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-1858G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087881 | ||||||
| chr10:49087894
|
TTA | T | 33 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0039g0167others(30): Show | 33 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-1873_458-1872d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087894 | ||||||
| chr10:49087911
|
G | GTA | 4 | a0001c0001t0001g0087a0002c0002t0001g0088a0002c0002t0001g0119others(1): Show | 4 | NA18970.hp2 NA18993.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-1890_458-1889d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087911 | ||||||
| chr10:49087913
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.458-1915_458-1891d others(27): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087913 | ||||||
| chr10:49087927
|
GTAATATA others(2): Show |
G | 3 | a0001c0001t0008g0193a0001c0001t0008g0196a0001c0001t0048g0192 | 3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-1913_458-1905d others(11): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087927 | ||||||
| chr10:49087936
|
ATGTATAT others(20): Show |
A | 20 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0039g0167others(17): Show | 20 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.458-1940_458-1914d others(29): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087936 | ||||||
| chr10:49087975
|
A | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-1952T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087975 | ||||||
| chr10:49087976
|
T | C | 1 | a0001c0003t0004g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458-1953A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087976 | ||||||
| chr10:49087988
|
A | G | 3 | a0001c0001t0008g0193a0001c0001t0008g0196a0001c0001t0048g0192 | 3 | HG01070.hp1 HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-1965T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087988 | ||||||
| chr10:49087992
|
G | A | 134 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(131): Show | 140 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.458-1969C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087992 | ||||||
| chr10:49087995
|
T | C | 28 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0009g0028others(25): Show | 29 | HG00639.hp2 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-1972A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49087995 | ||||||
| chr10:49088299
|
T | G | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-2276A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088299 | ||||||
| chr10:49088336
|
C | A | 6 | a0001c0001t0001g0034a0001c0001t0003g0036a0001c0001t0022g0045others(3): Show | 6 | HG02056.hp2 HG02083.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-2313G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088336 | ||||||
| chr10:49088481
|
A | G | 14 | a0001c0001t0039g0167a0001c0001t0042g0014a0002c0002t0002g0156others(11): Show | 14 | HG00558.hp1 HG02717.hp2 HG03195.hp1 others(11): Show |
intron_variant | MODIFIER | c.458-2458T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088481 | ||||||
| chr10:49088571
|
A | G | 3 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0014g0129 | 3 | NA18955.hp1 NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.458-2548T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088571 | ||||||
| chr10:49088577
|
G | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(118): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.458-2554C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088577 | ||||||
| chr10:49088667
|
C | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0128a0002c0002t0012g0127 | 3 | HG01106.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.458-2644G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088667 | ||||||
| chr10:49088723
|
A | T | 8 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-2700T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088723 | ||||||
| chr10:49088846
|
C | A | 2 | a0001c0001t0003g0251a0001c0001t0003g0252 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458-2823G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088846 | ||||||
| chr10:49088867
|
G | A | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458-2844C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088867 | ||||||
| chr10:49088875
|
T | C | 1 | a0002c0002t0006g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.458-2852A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088875 | ||||||
| chr10:49088901
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-2878G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088901 | ||||||
| chr10:49088936
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-2913G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088936 | ||||||
| chr10:49088975
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-2952G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49088975 | ||||||
| chr10:49089104
|
T | C | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.458-3081A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089104 | ||||||
| chr10:49089182
|
G | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-3159C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089182 | ||||||
| chr10:49089265
|
C | G | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-3242G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089265 | ||||||
| chr10:49089352
|
C | T | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-3329G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089352 | ||||||
| chr10:49089390
|
T | G | 1 | a0001c0003t0004g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458-3367A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089390 | ||||||
| chr10:49089427
|
C | T | 22 | a0001c0001t0002g0182a0001c0001t0005g0006a0001c0001t0005g0007others(19): Show | 24 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.458-3404G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089427 | ||||||
| chr10:49089495
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-3472G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089495 | ||||||
| chr10:49089520
|
C | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-3497G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089520 | ||||||
| chr10:49089662
|
C | T | 1 | a0002c0002t0003g0109 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.458-3639G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089662 | ||||||
| chr10:49089663
|
T | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458-3640A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089663 | ||||||
| chr10:49089767
|
G | T | 52 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(49): Show | 56 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.458-3744C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49089767 | ||||||
| chr10:49090014
|
G | A | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.458-3991C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090014 | ||||||
| chr10:49090038
|
T | C | 1 | a0002c0002t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.458-4015A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090038 | ||||||
| chr10:49090146
|
G | T | 22 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.458-4123C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090146 | ||||||
| chr10:49090305
|
G | A | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-4282C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090305 | ||||||
| chr10:49090476
|
A | G | 104 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(101): Show | 110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-4453T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090476 | ||||||
| chr10:49090494
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-4471C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090494 | ||||||
| chr10:49090524
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-4501A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090524 | ||||||
| chr10:49090690
|
C | T | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-4667G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090690 | ||||||
| chr10:49090836
|
G | C | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-4813C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090836 | ||||||
| chr10:49090884
|
C | T | 1 | a0002c0002t0016g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.458-4861G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090884 | ||||||
| chr10:49090987
|
C | T | 1 | a0002c0002t0003g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.458-4964G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49090987 | ||||||
| chr10:49091016
|
C | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-4993G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091016 | ||||||
| chr10:49091016
|
C | G | 157 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0221others(154): Show | 165 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.458-4993G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091016 | ||||||
| chr10:49091117
|
G | A | 1 | a0002c0002t0030g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.458-5094C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091117 | ||||||
| chr10:49091156
|
G | C | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.458-5133C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091156 | ||||||
| chr10:49091588
|
A | G | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-5565T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091588 | ||||||
| chr10:49091602
|
C | G | 1 | a0002c0002t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.458-5579G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091602 | ||||||
| chr10:49091634
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-5611G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091634 | ||||||
| chr10:49091913
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-5890C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091913 | ||||||
| chr10:49091914
|
GA | G | 4 | a0001c0005t0001g0176a0001c0005t0009g0174a0001c0005t0009g0175others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-5892delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091914 | ||||||
| chr10:49091975
|
G | A | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-5952C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49091975 | ||||||
| chr10:49092134
|
C | A | 104 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(101): Show | 110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-6111G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092134 | ||||||
| chr10:49092135
|
T | A | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.458-6112A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092135 | ||||||
| chr10:49092201
|
C | T | 161 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(158): Show | 169 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.458-6178G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092201 | ||||||
| chr10:49092348
|
C | T | 104 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(101): Show | 110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-6325G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092348 | ||||||
| chr10:49092420
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.458-6397G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092420 | ||||||
| chr10:49092460
|
C | A | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-6437G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092460 | ||||||
| chr10:49092724
|
C | G | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-6701G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092724 | ||||||
| chr10:49092761
|
C | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458-6738G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092761 | ||||||
| chr10:49092968
|
A | T | 19 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(16): Show | 19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-6945T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49092968 | ||||||
| chr10:49093001
|
A | G | 8 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-6978T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093001 | ||||||
| chr10:49093009
|
C | T | 6 | a0001c0004t0007g0016a0001c0004t0007g0017a0001c0004t0007g0019others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-6986G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093009 | ||||||
| chr10:49093029
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(196): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.458-7006A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093029 | ||||||
| chr10:49093032
|
T | C | 56 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(53): Show | 58 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.458-7009A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093032 | ||||||
| chr10:49093044
|
G | C | 1 | a0001c0001t0041g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458-7021C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093044 | ||||||
| chr10:49093330
|
G | T | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-7307C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093330 | ||||||
| chr10:49093489
|
G | A | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7466C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093489 | ||||||
| chr10:49093620
|
T | C | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-7597A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093620 | ||||||
| chr10:49093687
|
T | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-7664A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093687 | ||||||
| chr10:49093704
|
A | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7681T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093704 | ||||||
| chr10:49093742
|
C | CT | 18 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.458-7720dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | ||||||
| chr10:49093742
|
C | CTT | 12 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(9): Show | 14 | HG00423.hp2 HG03195.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.458-7721_458-7720d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | ||||||
| chr10:49093742
|
C | CTTT | 12 | a0001c0001t0005g0049a0002c0002t0002g0156a0002c0002t0002g0157others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-7722_458-7720d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | ||||||
| chr10:49093742
|
CT | C | 19 | a0001c0001t0003g0252a0001c0001t0008g0193a0001c0001t0009g0028others(16): Show | 19 | HG00323.hp1 HG01070.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-7720delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | ||||||
| chr10:49093742
|
CTT | C | 55 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(52): Show | 60 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.458-7721_458-7720d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093742 | ||||||
| chr10:49093784
|
G | C | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-7761C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093784 | ||||||
| chr10:49093847
|
A | G | 29 | a0001c0001t0001g0013a0001c0001t0003g0011a0001c0001t0003g0250others(26): Show | 30 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.458-7824T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093847 | ||||||
| chr10:49093905
|
G | T | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-7882C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093905 | ||||||
| chr10:49093982
|
C | T | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-7959G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093982 | ||||||
| chr10:49093989
|
C | T | 13 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(10): Show | 13 | HG00558.hp1 HG03579.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-7966G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093989 | ||||||
| chr10:49093990
|
A | G | 177 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(174): Show | 186 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.458-7967T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49093990 | ||||||
| chr10:49094047
|
G | A | 1 | a0002c0002t0010g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.458-8024C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094047 | ||||||
| chr10:49094135
|
G | A | 1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.458-8112C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094135 | ||||||
| chr10:49094160
|
CA | C | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-8138delT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094160 | ||||||
| chr10:49094223
|
G | A | 2 | a0002c0002t0007g0099a0002c0002t0007g0101 | 2 | HG00323.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.458-8200C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094223 | ||||||
| chr10:49094251
|
T | A | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-8228A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094251 | ||||||
| chr10:49094536
|
A | G | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-8513T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094536 | ||||||
| chr10:49094662
|
A | G | 2 | a0001c0001t0005g0048a0001c0001t0005g0052 | 2 | NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.458-8639T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094662 | ||||||
| chr10:49094769
|
ATTCTCAG others(2): Show |
A | 47 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(44): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.458-8755_458-8747d others(11): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094769 | ||||||
| chr10:49094787
|
T | C | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-8764A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094787 | ||||||
| chr10:49094792
|
G | C | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-8769C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094792 | ||||||
| chr10:49094795
|
G | T | 1 | a0001c0001t0028g0178 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.458-8772C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094795 | ||||||
| chr10:49094849
|
C | T | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-8826G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094849 | ||||||
| chr10:49094850
|
A | G | 161 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(158): Show | 169 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.458-8827T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094850 | ||||||
| chr10:49094911
|
C | G | 53 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(50): Show | 55 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-8888G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49094911 | ||||||
| chr10:49095044
|
A | C | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-9021T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095044 | ||||||
| chr10:49095107
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-9084C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095107 | ||||||
| chr10:49095129
|
C | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.458-9106G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095129 | ||||||
| chr10:49095410
|
C | T | 41 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0005g0006others(38): Show | 43 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.458-9387G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095410 | ||||||
| chr10:49095418
|
C | T | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(11): Show | 16 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.458-9395G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095418 | ||||||
| chr10:49095421
|
G | A | 48 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.458-9398C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095421 | ||||||
| chr10:49095491
|
C | T | 75 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(72): Show | 78 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.458-9468G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095491 | ||||||
| chr10:49095532
|
G | A | 9 | a0001c0003t0004g0200a0001c0003t0004g0202a0001c0003t0004g0204others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.458-9509C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095532 | ||||||
| chr10:49095594
|
T | C | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-9571A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095594 | ||||||
| chr10:49095751
|
T | C | 1 | a0001c0001t0011g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458-9728A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095751 | ||||||
| chr10:49095802
|
C | G | 1 | a0002c0002t0006g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-9779G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49095802 | ||||||
| chr10:49096013
|
T | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-9990A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096013 | ||||||
| chr10:49096334
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10311C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096334 | ||||||
| chr10:49096412
|
A | G | 1 | a0001c0001t0009g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458-10389T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096412 | ||||||
| chr10:49096468
|
G | A | 1 | a0001c0001t0011g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458-10445C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096468 | ||||||
| chr10:49096494
|
A | C | 7 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(4): Show | 8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10471T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096494 | ||||||
| chr10:49096622
|
C | CGT | 56 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0023others(53): Show | 63 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.458-10601_458-1060 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGT | 29 | a0001c0001t0001g0034a0001c0001t0002g0015a0001c0001t0002g0037others(26): Show | 29 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-10603_458-1060 others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGT | 33 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0002g0003others(30): Show | 36 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.458-10605_458-1060 others(10): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(1): Show |
20 | a0001c0001t0002g0219a0001c0001t0002g0222a0001c0001t0002g0235others(17): Show | 21 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.458-10607_458-1060 others(12): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(3): Show |
6 | a0001c0001t0009g0028a0001c0003t0004g0172a0001c0003t0004g0209others(3): Show | 6 | HG01884.hp1 HG02602.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-10609_458-1060 others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(5): Show |
8 | a0001c0001t0003g0018a0001c0001t0009g0027a0001c0001t0011g0183others(5): Show | 8 | HG00639.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10611_458-1060 others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0003g0207a0001c0003t0004g0208 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.458-10613_458-1060 others(18): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(9): Show |
5 | a0001c0001t0011g0205a0001c0003t0004g0206a0001c0003t0004g0213others(2): Show | 5 | HG02451.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-10615_458-1060 others(20): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(11): Show |
4 | a0001c0003t0004g0203a0001c0003t0004g0204a0001c0003t0004g0211others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-10617_458-1060 others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(15): Show |
3 | a0001c0003t0004g0202a0001c0003t0004g0210a0001c0003t0044g0201 | 3 | HG01109.hp1 HG01981.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.458-10621_458-1060 others(26): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
C | CGTGTGTG others(17): Show |
1 | a0001c0003t0004g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.458-10623_458-1060 others(28): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
CGT | C | 6 | a0001c0001t0002g0218a0001c0001t0005g0055a0001c0001t0008g0197others(3): Show | 6 | HG00099.hp1 HG02015.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-10601_458-1060 others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
CGTGT | C | 10 | a0001c0001t0003g0258a0001c0001t0042g0014a0001c0005t0001g0176others(7): Show | 10 | HG02135.hp2 HG02273.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-10603_458-1060 others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
CGTGTGT | C | 8 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-10605_458-1060 others(10): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
CGTGTGTG others(5): Show |
C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458-10611_458-1060 others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096622
|
CGTGTGTG others(11): Show |
C | 1 | a0002c0002t0008g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.458-10617_458-1060 others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096622 | ||||||
| chr10:49096677
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.458-10654C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096677 | ||||||
| chr10:49096749
|
G | A | 13 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(10): Show | 15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-10726C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096749 | ||||||
| chr10:49096804
|
G | A | 2 | a0002c0002t0001g0090a0002c0002t0001g0149 | 2 | HG02273.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.458-10781C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096804 | ||||||
| chr10:49096921
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(57): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.457+10673T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096921 | ||||||
| chr10:49096953
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.457+10641T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096953 | ||||||
| chr10:49096971
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(103): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.457+10623T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49096971 | ||||||
| chr10:49097150
|
C | T | 1 | a0001c0001t0019g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.457+10444G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097150 | ||||||
| chr10:49097194
|
C | A | 1 | a0002c0002t0001g0150 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.457+10400G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097194 | ||||||
| chr10:49097209
|
T | C | 1 | a0002c0002t0003g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.457+10385A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097209 | ||||||
| chr10:49097350
|
C | T | 12 | a0002c0002t0002g0156a0002c0002t0002g0157a0002c0002t0003g0109others(9): Show | 12 | HG00558.hp1 HG03704.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+10244G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097350 | ||||||
| chr10:49097450
|
T | TA | 46 | a0001c0001t0003g0011a0001c0001t0003g0207a0001c0001t0003g0250others(43): Show | 49 | HG00423.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.457+10143dupT | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097450 | ||||||
| chr10:49097635
|
G | A | 2 | a0001c0001t0011g0188a0001c0001t0024g0187 | 2 | HG00642.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.457+9959C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097635 | ||||||
| chr10:49097645
|
T | C | 1 | a0001c0001t0002g0235 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.457+9949A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097645 | ||||||
| chr10:49097834
|
G | T | 1 | a0001c0003t0043g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457+9760C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097834 | ||||||
| chr10:49097977
|
C | T | 42 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 43 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.457+9617G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49097977 | ||||||
| chr10:49098084
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+9510G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098084 | ||||||
| chr10:49098085
|
T | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+9509A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098085 | ||||||
| chr10:49098152
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+9442C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098152 | ||||||
| chr10:49098341
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 28 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+9253G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098341 | ||||||
| chr10:49098353
|
T | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+9241A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098353 | ||||||
| chr10:49098409
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01192.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.457+9185T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098409 | ||||||
| chr10:49098445
|
T | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+9149A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098445 | ||||||
| chr10:49098603
|
G | A | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+8991C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098603 | ||||||
| chr10:49098691
|
A | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(260): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.457+8903T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098691 | ||||||
| chr10:49098703
|
T | C | 1 | a0001c0001t0028g0178 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.457+8891A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098703 | ||||||
| chr10:49098778
|
C | T | 5 | a0001c0003t0004g0211a0001c0003t0004g0212a0001c0003t0004g0213others(2): Show | 5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+8816G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098778 | ||||||
| chr10:49098889
|
A | G | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+8705T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49098889 | ||||||
| chr10:49099072
|
C | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(28): Show | 34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.457+8522G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099072 | ||||||
| chr10:49099202
|
A | C | 15 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(12): Show | 15 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+8392T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099202 | ||||||
| chr10:49099229
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.457+8365C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099229 | ||||||
| chr10:49099241
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 28 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.457+8353G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099241 | ||||||
| chr10:49099257
|
A | G | 44 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(41): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+8337T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099257 | ||||||
| chr10:49099264
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+8330G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099264 | ||||||
| chr10:49099314
|
A | G | 4 | a0001c0001t0001g0221a0001c0001t0002g0220a0001c0001t0002g0244others(1): Show | 4 | HG02615.hp1 HG02738.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+8280T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099314 | ||||||
| chr10:49099397
|
G | A | 1 | a0001c0001t0029g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+8197C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099397 | ||||||
| chr10:49099415
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.457+8179A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099415 | ||||||
| chr10:49099416
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+8178G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099416 | ||||||
| chr10:49099431
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(86): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.457+8163T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099431 | ||||||
| chr10:49099738
|
A | G | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.457+7856T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099738 | ||||||
| chr10:49099898
|
C | T | 1 | a0002c0002t0002g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457+7696G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099898 | ||||||
| chr10:49099971
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+7623T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49099971 | ||||||
| chr10:49100024
|
A | G | 1 | a0001c0001t0019g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.457+7570T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100024 | ||||||
| chr10:49100072
|
AAGAGATA others(5): Show |
A | 19 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(16): Show | 19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+7510_457+7521d others(14): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100072 | ||||||
| chr10:49100142
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+7452G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100142 | ||||||
| chr10:49100446
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(56): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.457+7148G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100446 | ||||||
| chr10:49100475
|
G | A | 44 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(41): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+7119C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100475 | ||||||
| chr10:49100569
|
A | T | 13 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(10): Show | 15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+7025T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100569 | ||||||
| chr10:49100578
|
C | T | 1 | a0001c0001t0005g0006 | 2 | NA18966.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.457+7016G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100578 | ||||||
| chr10:49100796
|
G | GAC | 103 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+6797_457+6798i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100796 | ||||||
| chr10:49100833
|
T | C | 1 | a0001c0001t0003g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.457+6761A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100833 | ||||||
| chr10:49100855
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.457+6739A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49100855 | ||||||
| chr10:49101021
|
A | G | 1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.457+6573T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101021 | ||||||
| chr10:49101069
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.457+6525T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101069 | ||||||
| chr10:49101097
|
T | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+6497A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101097 | ||||||
| chr10:49101183
|
C | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+6411G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101183 | ||||||
| chr10:49101285
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.457+6309A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101285 | ||||||
| chr10:49101339
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+6255C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101339 | ||||||
| chr10:49101653
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+5941T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101653 | ||||||
| chr10:49101804
|
A | G | 15 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(12): Show | 15 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+5790T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101804 | ||||||
| chr10:49101824
|
G | T | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+5770C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101824 | ||||||
| chr10:49101860
|
T | C | 44 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(41): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+5734A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101860 | ||||||
| chr10:49101930
|
T | A | 19 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(16): Show | 19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+5664A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101930 | ||||||
| chr10:49101968
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+5626A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101968 | ||||||
| chr10:49101972
|
CGT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0034others(101): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.457+5620_457+5621d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101972 | ||||||
| chr10:49101975
|
G | C | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+5619C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101975 | ||||||
| chr10:49101983
|
GTGTGTT | G | 29 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(26): Show | 29 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457+5605_457+5610d others(8): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101983 | ||||||
| chr10:49101985
|
GTGTT | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01192.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+5605_457+5608d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101985 | ||||||
| chr10:49101987
|
GTT | G | 7 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(4): Show | 8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+5605_457+5606d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49101987 | ||||||
| chr10:49102160
|
GT | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(188): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.457+5433delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102160 | ||||||
| chr10:49102175
|
AG | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(55): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.457+5418delC | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102175 | ||||||
| chr10:49102178
|
G | A | 1 | a0002c0002t0049g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.457+5416C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102178 | ||||||
| chr10:49102182
|
T | TCTCGCTC others(10): Show |
58 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(55): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.457+5411_457+5412i others(19): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102182 | ||||||
| chr10:49102206
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(158): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.457+5388A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102206 | ||||||
| chr10:49102359
|
C | G | 1 | a0001c0001t0040g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.457+5235G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102359 | ||||||
| chr10:49102385
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.457+5209G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102385 | ||||||
| chr10:49102386
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.457+5208C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102386 | ||||||
| chr10:49102727
|
C | A | 12 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0049others(9): Show | 14 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.457+4867G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102727 | ||||||
| chr10:49102736
|
C | T | 1 | a0001c0005t0009g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.457+4858G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102736 | ||||||
| chr10:49102896
|
G | A | 1 | a0002c0002t0007g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.457+4698C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102896 | ||||||
| chr10:49102929
|
C | G | 2 | a0002c0002t0002g0156a0002c0002t0002g0157 | 2 | NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.457+4665G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102929 | ||||||
| chr10:49102996
|
G | A | 5 | a0001c0001t0002g0219a0001c0005t0001g0176a0001c0005t0009g0174others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+4598C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49102996 | ||||||
| chr10:49103005
|
A | T | 4 | a0001c0005t0001g0176a0001c0005t0009g0174a0001c0005t0009g0175others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+4589T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103005 | ||||||
| chr10:49103091
|
T | G | 7 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(4): Show | 8 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+4503A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103091 | ||||||
| chr10:49103296
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(46): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+4298T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103296 | ||||||
| chr10:49103328
|
G | A | 2 | a0002c0002t0006g0057a0002c0002t0006g0058 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.457+4266C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103328 | ||||||
| chr10:49103856
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+3738C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103856 | ||||||
| chr10:49103895
|
G | C | 1 | a0001c0001t0029g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+3699C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103895 | ||||||
| chr10:49103963
|
A | G | 1 | a0001c0001t0019g0181 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.457+3631T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103963 | ||||||
| chr10:49103974
|
C | T | 1 | a0005c0009t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+3620G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103974 | ||||||
| chr10:49103983
|
G | C | 14 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(11): Show | 14 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+3611C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49103983 | ||||||
| chr10:49104053
|
C | T | 1 | a0001c0001t0023g0033 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.457+3541G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104053 | ||||||
| chr10:49104064
|
C | G | 1 | a0001c0003t0043g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457+3530G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104064 | ||||||
| chr10:49104065
|
G | A | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.457+3529C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104065 | ||||||
| chr10:49104277
|
A | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(143): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.457+3317T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104277 | ||||||
| chr10:49104304
|
A | AAAC | 49 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(46): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+3287_457+3289d others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104304 | ||||||
| chr10:49104327
|
A | T | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.457+3267T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104327 | ||||||
| chr10:49104338
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.457+3256T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104338 | ||||||
| chr10:49104415
|
C | T | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+3179G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104415 | ||||||
| chr10:49104416
|
G | A | 1 | a0002c0002t0006g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.457+3178C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104416 | ||||||
| chr10:49104464
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+3130T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104464 | ||||||
| chr10:49104466
|
C | A | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.457+3128G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104466 | ||||||
| chr10:49104522
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(46): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+3072A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104522 | ||||||
| chr10:49104531
|
G | A | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+3063C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104531 | ||||||
| chr10:49104685
|
G | A | 19 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0003t0004g0172others(16): Show | 19 | HG01109.hp1 HG01123.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+2909C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104685 | ||||||
| chr10:49104726
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.457+2868C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104726 | ||||||
| chr10:49104761
|
A | T | 1 | a0001c0001t0002g0219 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.457+2833T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104761 | ||||||
| chr10:49104792
|
C | G | 1 | a0001c0001t0019g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.457+2802G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104792 | ||||||
| chr10:49104804
|
TAGAG | T | 53 | a0001c0001t0002g0182a0001c0001t0003g0011a0001c0001t0003g0207others(50): Show | 56 | HG00423.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.457+2786_457+2789d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104804 | ||||||
| chr10:49104830
|
CAG | C | 9 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(6): Show | 9 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.457+2762_457+2763d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104830 | ||||||
| chr10:49104859
|
A | T | 1 | a0002c0002t0002g0156 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.457+2735T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104859 | ||||||
| chr10:49104860
|
C | T | 26 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(23): Show | 29 | HG00423.hp2 HG01069.hp1 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.457+2734G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104860 | ||||||
| chr10:49104886
|
AAG | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(98): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.457+2706_457+2707d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104886 | ||||||
| chr10:49104957
|
AGAGACAG others(13): Show |
A | 1 | a0001c0001t0002g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.457+2617_457+2636d others(22): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104957 | ||||||
| chr10:49104962
|
CAG | C | 43 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(40): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.457+2630_457+2631d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104962 | ||||||
| chr10:49104966
|
G | C | 1 | a0001c0003t0004g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.457+2628C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104966 | ||||||
| chr10:49104998
|
CAG | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2594_457+2595d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49104998 | ||||||
| chr10:49105010
|
C | G | 26 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0011g0205others(23): Show | 26 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.457+2584G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105010 | ||||||
| chr10:49105034
|
C | CA | 263 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(260): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.457+2559_457+2560i others(3): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105034 | ||||||
| chr10:49105067
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2527C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105067 | ||||||
| chr10:49105159
|
AAGAG | A | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+2431_457+2434d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105159 | ||||||
| chr10:49105213
|
C | CAG | 77 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(74): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.457+2379_457+2380d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | ||||||
| chr10:49105213
|
C | CAGAG | 50 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(47): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.457+2377_457+2380d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | ||||||
| chr10:49105213
|
CAG | C | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0049others(11): Show | 16 | HG00423.hp2 HG02970.hp1 HG03540.hp1 others(13): Show |
intron_variant | MODIFIER | c.457+2379_457+2380d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105213 | ||||||
| chr10:49105260
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(99): Show | 112 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.457+2334G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105260 | ||||||
| chr10:49105292
|
A | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.457+2302T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105292 | ||||||
| chr10:49105329
|
C | CAG | 19 | a0001c0001t0003g0217a0001c0001t0008g0189a0001c0001t0008g0190others(16): Show | 19 | HG00099.hp1 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | ||||||
| chr10:49105329
|
C | CAGA | 66 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(63): Show | 71 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(5): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | ||||||
| chr10:49105329
|
C | CAGAG | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | ||||||
| chr10:49105329
|
C | CAGAGA | 45 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(42): Show | 50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.457+2264_457+2265i others(7): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105329 | ||||||
| chr10:49105330
|
G | A | 28 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(25): Show | 29 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457+2264C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105330 | ||||||
| chr10:49105331
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(42): Show | 50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.457+2263C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105331 | ||||||
| chr10:49105331
|
G | T | 1 | a0001c0004t0007g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.457+2263C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105331 | ||||||
| chr10:49105332
|
G | A | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+2262C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105332 | ||||||
| chr10:49105392
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.457+2202C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105392 | ||||||
| chr10:49105576
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(142): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.457+2018C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105576 | ||||||
| chr10:49105656
|
T | C | 13 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(10): Show | 15 | HG00423.hp2 NA18941.hp2 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1938A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105656 | ||||||
| chr10:49105699
|
G | A | 44 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(41): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.457+1895C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105699 | ||||||
| chr10:49105807
|
A | C | 7 | a0001c0001t0011g0012a0001c0001t0011g0183a0001c0001t0011g0186others(4): Show | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+1787T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105807 | ||||||
| chr10:49105822
|
A | G | 1 | a0001c0001t0042g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.457+1772T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105822 | ||||||
| chr10:49105828
|
CAT | C | 43 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(40): Show | 47 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.457+1764_457+1765d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105828 | ||||||
| chr10:49105835
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+1759C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105835 | ||||||
| chr10:49105841
|
G | GTA | 35 | a0001c0001t0003g0018a0001c0001t0008g0193a0001c0001t0008g0194others(32): Show | 36 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.457+1751_457+1752d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | ||||||
| chr10:49105841
|
G | GTATA | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01192.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+1749_457+1752d others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | ||||||
| chr10:49105841
|
GTA | G | 17 | a0002c0002t0001g0090a0002c0002t0002g0096a0002c0002t0006g0057others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.457+1751_457+1752d others(4): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105841 | ||||||
| chr10:49105843
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457+1751T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49105843 | ||||||
| chr10:49106133
|
G | T | 1 | a0001c0001t0047g0248 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.457+1461C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106133 | ||||||
| chr10:49106582
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+1012C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106582 | ||||||
| chr10:49106696
|
A | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457+898T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106696 | ||||||
| chr10:49106742
|
C | G | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+852G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106742 | ||||||
| chr10:49106976
|
C | G | 1 | a0002c0002t0001g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.457+618G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49106976 | ||||||
| chr10:49107035
|
C | G | 97 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(94): Show | 104 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.457+559G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107035 | ||||||
| chr10:49107050
|
T | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 30 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.457+544A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107050 | ||||||
| chr10:49107189
|
G | A | 1 | a0001c0003t0004g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.457+405C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107189 | ||||||
| chr10:49107301
|
G | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457+293C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107301 | ||||||
| chr10:49107323
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457+271C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107323 | ||||||
| chr10:49107358
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0042g0014 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.457+236C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107358 | ||||||
| chr10:49107390
|
G | A | 1 | a0001c0001t0029g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+204C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107390 | ||||||
| chr10:49107487
|
T | C | 1 | a0002c0002t0001g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.457+107A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107487 | ||||||
| chr10:49107541
|
G | T | 1 | a0002c0002t0001g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.457+53C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 2/7 | chr10 | 49107541 | ||||||
| chr10:49108182
|
C | T | 1 | a0001c0003t0004g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-187G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108182 | ||||||
| chr10:49108471
|
G | C | 1 | a0001c0001t0002g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.56-476C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108471 | ||||||
| chr10:49108538
|
C | G | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.56-543G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108538 | ||||||
| chr10:49108541
|
C | T | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-546G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108541 | ||||||
| chr10:49108573
|
A | T | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-578T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108573 | ||||||
| chr10:49108636
|
G | A | 2 | a0001c0001t0021g0241a0001c0001t0021g0242 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.56-641C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108636 | ||||||
| chr10:49108948
|
C | T | 4 | a0002c0002t0001g0075a0002c0002t0013g0008a0002c0002t0013g0073others(1): Show | 5 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-953G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49108948 | ||||||
| chr10:49109106
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0048others(7): Show | 12 | NA18941.hp2 NA18947.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.56-1111G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109106 | ||||||
| chr10:49109269
|
G | A | 1 | a0002c0002t0001g0044 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.56-1274C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109269 | ||||||
| chr10:49109348
|
G | A | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.56-1353C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109348 | ||||||
| chr10:49109356
|
G | A | 1 | a0002c0002t0032g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-1361C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109356 | ||||||
| chr10:49109364
|
G | C | 1 | a0001c0001t0002g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.56-1369C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109364 | ||||||
| chr10:49109474
|
A | ATG | 118 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.56-1481_56-1480dup others(2): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109474 | ||||||
| chr10:49109488
|
A | AT | 81 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(78): Show | 85 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.56-1494dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109488 | ||||||
| chr10:49109601
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.56-1606T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109601 | ||||||
| chr10:49109604
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.56-1609A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109604 | ||||||
| chr10:49109606
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.56-1611T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109606 | ||||||
| chr10:49109618
|
C | G | 4 | a0001c0005t0001g0176a0001c0005t0009g0174a0001c0005t0009g0175others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-1623G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109618 | ||||||
| chr10:49109695
|
G | T | 1 | a0001c0001t0020g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.56-1700C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109695 | ||||||
| chr10:49109733
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.56-1738G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109733 | ||||||
| chr10:49109793
|
C | G | 1 | a0001c0001t0005g0061 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.56-1798G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109793 | ||||||
| chr10:49109795
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.56-1800G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109795 | ||||||
| chr10:49109980
|
C | T | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56-1985G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49109980 | ||||||
| chr10:49110046
|
G | C | 13 | a0002c0002t0002g0155a0002c0002t0002g0156a0002c0002t0002g0157others(10): Show | 13 | HG00558.hp1 HG03704.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-2051C>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110046 | ||||||
| chr10:49110064
|
C | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.56-2069G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110064 | ||||||
| chr10:49110096
|
C | T | 113 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(110): Show | 118 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.56-2101G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110096 | ||||||
| chr10:49110401
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.56-2406A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110401 | ||||||
| chr10:49110439
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.56-2444C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110439 | ||||||
| chr10:49110455
|
AT | A | 4 | a0001c0001t0003g0257a0001c0001t0003g0259a0001c0001t0020g0256others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-2461delA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110455 | ||||||
| chr10:49110479
|
A | G | 3 | a0002c0002t0017g0070a0002c0002t0017g0071a0002c0002t0017g0072 | 3 | HG02622.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.56-2484T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110479 | ||||||
| chr10:49110567
|
G | A | 5 | a0001c0003t0004g0211a0001c0003t0004g0212a0001c0003t0004g0213others(2): Show | 5 | HG01123.hp1 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-2572C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110567 | ||||||
| chr10:49110673
|
G | T | 7 | a0001c0001t0011g0183a0001c0001t0011g0186a0001c0001t0011g0188others(4): Show | 7 | HG00642.hp1 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-2678C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49110673 | ||||||
| chr10:49111278
|
C | T | 9 | a0001c0001t0005g0061a0001c0001t0005g0062a0001c0001t0005g0063others(6): Show | 9 | HG00423.hp2 HG01346.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-3283G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111278 | ||||||
| chr10:49111342
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(145): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.56-3347C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111342 | ||||||
| chr10:49111583
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.56-3588C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111583 | ||||||
| chr10:49111654
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0011g0012a0001c0001t0042g0014 | 3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3659G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111654 | ||||||
| chr10:49111740
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3691G>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111740 | ||||||
| chr10:49111831
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3600G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111831 | ||||||
| chr10:49111883
|
C | T | 18 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0038g0198others(15): Show | 18 | HG01109.hp1 HG01123.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3548G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111883 | ||||||
| chr10:49111919
|
GTGAGCT | G | 6 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+3506_55+3511del others(6): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111919 | ||||||
| chr10:49111920
|
T | G | 7 | a0001c0001t0002g0182a0001c0001t0018g0169a0001c0001t0018g0170others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3511A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111920 | ||||||
| chr10:49111995
|
G | A | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+3436C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49111995 | ||||||
| chr10:49112096
|
C | G | 1 | a0002c0002t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.55+3335G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112096 | ||||||
| chr10:49112210
|
A | C | 1 | a0001c0001t0038g0198 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.55+3221T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112210 | ||||||
| chr10:49112236
|
C | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3195G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112236 | ||||||
| chr10:49112466
|
T | C | 75 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(72): Show | 79 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.55+2965A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112466 | ||||||
| chr10:49112678
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.55+2753A>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112678 | ||||||
| chr10:49112842
|
T | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+2589A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112842 | ||||||
| chr10:49112990
|
C | G | 1 | a0001c0001t0039g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+2441G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49112990 | ||||||
| chr10:49113422
|
G | A | 9 | a0001c0001t0008g0189a0001c0001t0008g0190a0001c0001t0008g0191others(6): Show | 9 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+2009C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113422 | ||||||
| chr10:49113602
|
C | T | 1 | a0002c0002t0001g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.55+1829G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113602 | ||||||
| chr10:49113629
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.55+1802G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113629 | ||||||
| chr10:49113787
|
A | G | 48 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(45): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.55+1644T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113787 | ||||||
| chr10:49113873
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.55+1558G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113873 | ||||||
| chr10:49113949
|
G | A | 73 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(70): Show | 77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.55+1482C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49113949 | ||||||
| chr10:49114072
|
T | C | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.55+1359A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114072 | ||||||
| chr10:49114143
|
A | G | 1 | a0001c0001t0025g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.55+1288T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114143 | ||||||
| chr10:49114207
|
A | C | 1 | a0006c0011t0046g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.55+1224T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114207 | ||||||
| chr10:49114238
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.55+1193T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114238 | ||||||
| chr10:49114274
|
T | C | 3 | a0001c0001t0022g0045a0001c0001t0022g0047a0001c0001t0023g0046 | 3 | HG02056.hp2 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.55+1157A>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114274 | ||||||
| chr10:49114398
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.55+1033T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114398 | ||||||
| chr10:49114413
|
G | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 34 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.55+1018C>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114413 | ||||||
| chr10:49114434
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.55+997T>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114434 | ||||||
| chr10:49114435
|
A | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(146): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.55+996T>G | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114435 | ||||||
| chr10:49114482
|
G | A | 1 | a0002c0002t0003g0166 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.55+949C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114482 | ||||||
| chr10:49114503
|
G | A | 18 | a0001c0001t0003g0207a0001c0001t0011g0205a0001c0001t0038g0198others(15): Show | 18 | HG01109.hp1 HG01123.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+928C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114503 | ||||||
| chr10:49114512
|
T | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.55+919A>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114512 | ||||||
| chr10:49114585
|
G | GT | 16 | a0001c0001t0001g0013a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 18 | HG00642.hp2 HG00741.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.55+845dupA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | ||||||
| chr10:49114585
|
G | GTT | 38 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0008g0189others(35): Show | 38 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.55+844_55+845dupAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | ||||||
| chr10:49114585
|
G | GTTT | 16 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(13): Show | 19 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.55+843_55+845dupAA others(1): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | ||||||
| chr10:49114585
|
G | GTTTTT | 11 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(8): Show | 12 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.55+841_55+845dupAA others(3): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | ||||||
| chr10:49114585
|
GTT | G | 6 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+844_55+845delAA | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114585 | ||||||
| chr10:49114587
|
T | TTTG | 51 | a0001c0001t0001g0034a0001c0001t0001g0221a0001c0001t0001g0231others(48): Show | 55 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.55+843_55+844insCA others(1): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114587 | ||||||
| chr10:49114639
|
G | A | 13 | a0001c0001t0003g0011a0001c0001t0003g0250a0001c0001t0003g0251others(10): Show | 14 | HG01069.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+792C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114639 | ||||||
| chr10:49114657
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0221others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.55+774C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114657 | ||||||
| chr10:49114730
|
C | T | 16 | a0001c0001t0001g0034a0001c0001t0002g0035a0001c0001t0002g0037others(13): Show | 16 | HG00597.hp1 HG00621.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+701G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114730 | ||||||
| chr10:49114734
|
C | CCCTGCTG others(11): Show |
6 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+679_55+696dupCT others(16): Show |
VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114734 | ||||||
| chr10:49114888
|
C | T | 6 | a0001c0001t0003g0018a0001c0004t0007g0016a0001c0004t0007g0017others(3): Show | 7 | HG00639.hp2 HG03041.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+543G>A | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49114888 | ||||||
| chr10:49115007
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.55+424C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115007 | ||||||
| chr10:49115167
|
C | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+264G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115167 | ||||||
| chr10:49115266
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.55+165T>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115266 | ||||||
| chr10:49115303
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 7 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+128C>T | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115303 | ||||||
| chr10:49115393
|
C | G | 3 | a0001c0001t0001g0013a0001c0001t0011g0012a0001c0001t0042g0014 | 3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+38G>C | VSTM4 | ENSG00000165633.13 | transcript | ENST00000332853.9 | protein_coding | 1/7 | chr10 | 49115393 |