| geneid | 389337 |
|---|---|
| ensemblid | ENSG00000183111.12 |
| hgncid | 34430 |
| symbol | ARHGEF37 |
| name | Rho guanine nucleotide exchange factor 37 |
| refseq_nuc | NM_001001669.3 |
| refseq_prot | NP_001001669.2 |
| ensembl_nuc | ENST00000333677.7 |
| ensembl_prot | ENSP00000328083.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 149581498 |
| end | 149634968 |
| strand | + |
| ver | v1.2 |
| region | chr5:149581498-149634968 |
| region5000 | chr5:149576498-149639968 |
| regionname0 | ARHGEF37_chr5_149581498_149634968 |
| regionname5000 | ARHGEF37_chr5_149576498_149639968 |
| 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 | 0/0 | 675 | 96 | 17 | 14 | 42 | 11 | 12 | 36 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002 | 0/1 | 675 | 74 | 5 | 21 | 33 | 4 | 10 | 24 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003 | 0/0 | 675 | 67 | 2 | 10 | 52 | 2 | 1 | 40 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004 | 0/0 | 675 | 55 | 23 | 4 | 23 | 1 | 4 | 18 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005 | 0/0 | 675 | 24 | 7 | 0 | 16 | 0 | 1 | 13 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006 | 0/0 | 675 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0007 | 0/0 | 675 | 14 | 0 | 0 | 14 | 0 | 0 | 12 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008 | 0/0 | 675 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0009 | 0/0 | 675 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0010 | 0/0 | 675 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0011 | 0/0 | 675 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0012 | 0/0 | 675 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0013 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0014 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0015 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0016 | 0/0 | 675 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0017 | 0/0 | 675 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0018 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0019 | 0/0 | 675 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0020 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0021 | 0/0 | 320 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0022 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0023 | 1/0 | 675 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0024 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| 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 | 2028 | 72 | 5 | 20 | 33 | 4 | 9 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0002 | 0/0 | 2028 | 61 | 9 | 3 | 41 | 4 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0003 | 0/0 | 2028 | 60 | 2 | 10 | 46 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0004 | 0/0 | 2028 | 47 | 16 | 4 | 22 | 1 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0005 | 0/0 | 2028 | 34 | 8 | 11 | 0 | 7 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0006 | 0/0 | 2028 | 16 | 16 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0007 | 0/0 | 2028 | 15 | 0 | 0 | 14 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0008 | 0/0 | 2028 | 14 | 0 | 0 | 14 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0009 | 0/0 | 2028 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0010 | 0/0 | 2028 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0011 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0012 | 0/0 | 2028 | 6 | 0 | 0 | 5 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0013 | 0/0 | 2028 | 5 | 2 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0014 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0015 | 0/0 | 2028 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0016 | 0/0 | 2028 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0017 | 0/0 | 2028 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0018 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0019 | 0/0 | 2028 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0020 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0021 | 0/0 | 2028 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0022 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0023 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0024 | 0/0 | 2028 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0025 | 0/0 | 2028 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0026 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0027 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0028 | 1/0 | 2028 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0029 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0030 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0031 | 0/0 | 2028 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0032 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0033 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0034 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0035 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0036 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| c0037 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| 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 | 0/1 | 2916 | 78 | 5 | 16 | 44 | 3 | 9 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0002 | 0/0 | 2916 | 65 | 3 | 9 | 49 | 2 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0003 | 1/0 | 2916 | 45 | 10 | 7 | 23 | 1 | 3 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0004 | 0/0 | 2916 | 42 | 12 | 4 | 23 | 1 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0005 | 0/0 | 2916 | 34 | 2 | 13 | 0 | 9 | 10 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0006 | 0/0 | 2916 | 34 | 1 | 2 | 25 | 2 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0007 | 0/0 | 2916 | 16 | 16 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0008 | 0/0 | 2916 | 14 | 1 | 0 | 13 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0009 | 0/0 | 2916 | 13 | 13 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0010 | 0/0 | 2916 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0011 | 0/0 | 2916 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0012 | 0/0 | 2916 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0013 | 0/0 | 2916 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0014 | 0/0 | 2916 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0015 | 0/0 | 2916 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0016 | 0/0 | 2916 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0017 | 0/0 | 2916 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0018 | 0/0 | 2916 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0019 | 0/0 | 2916 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0020 | 0/0 | 2916 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0021 | 0/0 | 2916 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0022 | 0/0 | 2916 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0023 | 0/0 | 2916 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0024 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0025 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0026 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0027 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0028 | 0/0 | 2916 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0029 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0030 | 0/0 | 2916 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0031 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0032 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0033 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0034 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| t0035 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| 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 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2028 | 61 | 9 | 3 | 41 | 4 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0005 | 0/0 | 2028 | 34 | 8 | 11 | 0 | 7 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0030 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0001 | 0/1 | 2028 | 72 | 5 | 20 | 33 | 4 | 9 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0024 | 0/0 | 2028 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003 | 0/0 | 2028 | 60 | 2 | 10 | 46 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0012 | 0/0 | 2028 | 6 | 0 | 0 | 5 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0029 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004 | 0/0 | 2028 | 47 | 16 | 4 | 22 | 1 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0010 | 0/0 | 2028 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0036 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0007 | 0/0 | 2028 | 15 | 0 | 0 | 14 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0011 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0027 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0033 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0035 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0006 | 0/0 | 2028 | 16 | 16 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0023 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0007c0008 | 0/0 | 2028 | 14 | 0 | 0 | 14 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0009 | 0/0 | 2028 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0017 | 0/0 | 2028 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0009c0013 | 0/0 | 2028 | 5 | 2 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0010c0015 | 0/0 | 2028 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0011c0014 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0012c0016 | 0/0 | 2028 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0013c0026 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0014c0022 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0015c0018 | 0/0 | 2028 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0016c0025 | 0/0 | 2028 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0017c0021 | 0/0 | 2028 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0018c0020 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0019c0019 | 0/0 | 2028 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0020c0032 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0021c0034 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0022c0031 | 0/0 | 2028 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0023c0028 | 1/0 | 2028 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0024c0037 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0004 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0005 | 0/0 | 4943 | 4 | 0 | 0 | 0 | 2 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0006 | 0/0 | 4943 | 31 | 1 | 2 | 24 | 2 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0008 | 0/0 | 4943 | 13 | 1 | 0 | 12 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0010 | 0/0 | 4943 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0011 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0015 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0020 | 0/0 | 4943 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0002t0027 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0005t0004 | 0/0 | 4943 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0005t0005 | 0/0 | 4943 | 25 | 1 | 9 | 0 | 7 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0005t0019 | 0/0 | 4943 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0005t0029 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0001c0030t0006 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0001t0001 | 0/1 | 4943 | 62 | 2 | 16 | 32 | 3 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0001t0003 | 0/0 | 4943 | 9 | 2 | 4 | 1 | 1 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0001t0018 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0002c0024t0003 | 0/0 | 4943 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003t0002 | 0/0 | 4943 | 55 | 2 | 9 | 42 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003t0008 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003t0012 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003t0016 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0003t0018 | 0/0 | 4943 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0012t0002 | 0/0 | 4943 | 5 | 0 | 0 | 4 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0012t0012 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0003c0029t0002 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0002 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0004 | 0/0 | 4943 | 32 | 5 | 4 | 20 | 1 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0009 | 0/0 | 4943 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0024 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0028 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0030 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0004t0033 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0010t0009 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0010t0014 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0010t0022 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0004c0036t0004 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0007t0003 | 0/0 | 4943 | 15 | 0 | 0 | 14 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0011t0001 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0011t0003 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0027t0003 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0033t0003 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0005c0035t0003 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0006t0007 | 0/0 | 4943 | 14 | 14 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0006t0032 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0006t0034 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0006c0023t0007 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0007c0008t0001 | 0/0 | 4943 | 10 | 0 | 0 | 10 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0007c0008t0003 | 0/0 | 4943 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0009t0002 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0009t0003 | 0/0 | 4943 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0009t0025 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0009t0026 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0017t0013 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0008c0017t0031 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0009c0013t0011 | 0/0 | 4943 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0009c0013t0021 | 0/0 | 4943 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0010c0015t0005 | 0/0 | 4943 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0011c0014t0011 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0011c0014t0023 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0011c0014t0035 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0012c0016t0012 | 0/0 | 4943 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0013c0026t0003 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0014c0022t0004 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0015c0018t0001 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0016c0025t0013 | 0/0 | 4943 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0017c0021t0006 | 0/0 | 4943 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0018c0020t0017 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0019c0019t0002 | 0/0 | 4943 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0020c0032t0009 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0021c0034t0005 | 0/0 | 4943 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0022c0031t0001 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0023c0028t0003 | 1/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| a0024c0037t0003 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | copy fasta | chr5 | 149576498 | 149639968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0011g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0020g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0020g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0027g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0019g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0019g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0029g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0030t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0024t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0024t0003g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0008g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0016g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0016g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0018g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0029t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0024g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0028g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0030g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0033g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0009g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0009g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0022g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0022g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0036t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0027t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0033t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0035t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0032g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0034g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0023t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0023t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0025g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0026g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0011g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0021g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0021g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0014t0011g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0014t0023g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0014t0035g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0012c0016t0012g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0012c0016t0012g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0012c0016t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0013c0026t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0013c0026t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0014c0022t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0014c0022t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0015c0018t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0015c0018t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0016c0025t0013g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0016c0025t0013g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0017c0021t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0017c0021t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0018c0020t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0018c0020t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0019c0019t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0019c0019t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0020c0032t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0021c0034t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0022c0031t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0023c0028t0003g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0024c0037t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0005 | g0194 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0331 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0341 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0049 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00280 | hp1 | a0001 | c0005 | t0005 | g0187 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00280 | hp2 | a0004 | c0004 | t0004 | g0373 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00323 | hp1 | a0002 | c0001 | t0003 | g0217 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00323 | hp2 | a0001 | c0005 | t0005 | g0192 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00408 | hp1 | a0003 | c0029 | t0002 | g0273 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0125 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0287 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0043 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00438 | hp1 | a0004 | c0036 | t0004 | g0236 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00438 | hp2 | a0003 | c0003 | t0002 | g0315 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00544 | hp1 | a0001 | c0002 | t0008 | g0253 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00544 | hp2 | a0002 | c0001 | t0003 | g0165 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00558 | hp1 | a0013 | c0026 | t0003 | g0234 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00597 | hp1 | a0005 | c0007 | t0003 | g0151 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00597 | hp2 | a0004 | c0004 | t0004 | g0249 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00609 | hp1 | a0005 | c0007 | t0003 | g0160 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0031 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00621 | hp1 | a0007 | c0008 | t0001 | g0100 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00621 | hp2 | a0003 | c0003 | t0016 | g0290 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00639 | hp1 | a0001 | c0005 | t0005 | g0001 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00639 | hp2 | a0002 | c0001 | t0003 | g0371 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00673 | hp1 | a0014 | c0022 | t0004 | g0344 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00735 | hp1 | a0008 | c0009 | t0003 | g0323 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0332 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0106 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00738 | hp2 | a0001 | c0002 | t0020 | g0135 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0133 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00741 | hp2 | a0001 | c0005 | t0005 | g0197 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0299 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01069 | hp2 | a0009 | c0013 | t0011 | g0011 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01071 | hp1 | a0009 | c0013 | t0011 | g0011 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01071 | hp2 | a0001 | c0005 | t0005 | g0002 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01074 | hp1 | a0004 | c0004 | t0004 | g0375 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01074 | hp2 | a0001 | c0005 | t0005 | g0001 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01081 | hp1 | a0002 | c0001 | t0003 | g0295 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0248 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01099 | hp2 | a0001 | c0005 | t0005 | g0191 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01106 | hp1 | a0001 | c0005 | t0019 | g0195 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01106 | hp2 | a0003 | c0003 | t0018 | g0342 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0205 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01167 | hp2 | a0016 | c0025 | t0013 | g0262 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01169 | hp1 | a0021 | c0034 | t0005 | g0002 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01169 | hp2 | a0016 | c0025 | t0013 | g0263 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01175 | hp1 | a0002 | c0001 | t0003 | g0353 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0347 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01243 | hp1 | a0009 | c0013 | t0021 | g0108 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01243 | hp2 | a0004 | c0004 | t0004 | g0180 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0035 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01255 | hp2 | a0001 | c0005 | t0005 | g0199 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01256 | hp1 | a0010 | c0015 | t0005 | g0182 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0056 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0377 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01257 | hp2 | a0004 | c0004 | t0004 | g0013 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01258 | hp1 | a0004 | c0004 | t0004 | g0013 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01258 | hp2 | a0010 | c0015 | t0005 | g0183 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01261 | hp2 | a0001 | c0002 | t0006 | g0130 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0060 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01346 | hp2 | a0001 | c0005 | t0005 | g0247 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01358 | hp1 | a0001 | c0005 | t0019 | g0188 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0055 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0330 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0065 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0016 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01496 | hp1 | a0008 | c0009 | t0003 | g0322 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0021 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0066 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01515 | hp2 | a0001 | c0005 | t0005 | g0200 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01516 | hp1 | a0001 | c0002 | t0006 | g0129 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0367 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01517 | hp1 | a0001 | c0002 | t0006 | g0127 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0063 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01884 | hp1 | a0004 | c0010 | t0022 | g0041 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01884 | hp2 | a0004 | c0004 | t0009 | g0009 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01891 | hp1 | a0001 | c0005 | t0005 | g0190 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01891 | hp2 | a0018 | c0020 | t0017 | g0176 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01934 | hp1 | a0010 | c0015 | t0005 | g0203 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0074 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01943 | hp1 | a0002 | c0001 | t0003 | g0216 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01943 | hp2 | a0001 | c0005 | t0005 | g0193 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01952 | hp1 | a0003 | c0003 | t0002 | g0277 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01975 | hp1 | a0003 | c0003 | t0002 | g0279 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0280 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0057 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0019 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01993 | hp2 | a0002 | c0024 | t0003 | g0206 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02015 | hp1 | a0003 | c0003 | t0002 | g0345 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02015 | hp2 | a0003 | c0012 | t0002 | g0161 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02027 | hp1 | a0012 | c0016 | t0012 | g0053 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02027 | hp2 | a0005 | c0007 | t0003 | g0154 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02040 | hp1 | a0001 | c0002 | t0008 | g0167 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0292 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02055 | hp1 | a0001 | c0005 | t0004 | g0214 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02055 | hp2 | a0004 | c0004 | t0009 | g0267 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02071 | hp1 | a0001 | c0002 | t0006 | g0113 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02074 | hp1 | a0007 | c0008 | t0001 | g0101 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02074 | hp2 | a0003 | c0003 | t0002 | g0010 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02129 | hp1 | a0001 | c0002 | t0006 | g0117 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02129 | hp2 | a0014 | c0022 | t0004 | g0366 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02132 | hp1 | a0019 | c0019 | t0002 | g0283 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02132 | hp2 | a0004 | c0004 | t0004 | g0239 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02135 | hp1 | a0001 | c0002 | t0006 | g0045 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02135 | hp2 | a0003 | c0003 | t0012 | g0048 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02145 | hp1 | a0004 | c0004 | t0004 | g0244 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02145 | hp2 | a0002 | c0001 | t0018 | g0271 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02155 | hp1 | a0004 | c0004 | t0004 | g0231 | EAS | CDX | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0285 | EAS | CDX | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02257 | hp1 | a0004 | c0004 | t0004 | g0348 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02257 | hp2 | a0010 | c0015 | t0005 | g0207 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02280 | hp1 | a0006 | c0006 | t0007 | g0360 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02280 | hp2 | a0005 | c0011 | t0001 | g0037 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02451 | hp1 | a0006 | c0006 | t0007 | g0369 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02451 | hp2 | a0008 | c0009 | t0003 | g0320 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02523 | hp1 | a0003 | c0012 | t0002 | g0164 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02572 | hp1 | a0006 | c0006 | t0007 | g0362 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02572 | hp2 | a0004 | c0004 | t0009 | g0257 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02602 | hp1 | a0002 | c0024 | t0003 | g0378 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02602 | hp2 | a0003 | c0012 | t0002 | g0215 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02615 | hp1 | a0011 | c0014 | t0011 | g0275 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02615 | hp2 | a0005 | c0011 | t0003 | g0372 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02622 | hp1 | a0005 | c0011 | t0003 | g0324 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02622 | hp2 | a0006 | c0023 | t0007 | g0266 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02630 | hp1 | a0006 | c0006 | t0007 | g0354 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02630 | hp2 | a0005 | c0035 | t0003 | g0242 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02647 | hp1 | a0006 | c0006 | t0007 | g0358 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02647 | hp2 | a0001 | c0002 | t0011 | g0365 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0080 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02683 | hp2 | a0001 | c0002 | t0005 | g0374 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02717 | hp1 | a0004 | c0004 | t0009 | g0260 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0352 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02735 | hp1 | a0001 | c0005 | t0005 | g0185 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0054 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0076 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02738 | hp2 | a0001 | c0005 | t0005 | g0201 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02809 | hp1 | a0004 | c0004 | t0009 | g0259 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02809 | hp2 | a0008 | c0009 | t0026 | g0318 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02818 | hp1 | a0005 | c0011 | t0001 | g0039 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02818 | hp2 | a0004 | c0004 | t0004 | g0243 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02886 | hp1 | a0009 | c0013 | t0011 | g0329 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02886 | hp2 | a0001 | c0002 | t0008 | g0317 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02895 | hp1 | a0011 | c0014 | t0023 | g0003 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02895 | hp2 | a0005 | c0011 | t0001 | g0038 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02896 | hp1 | a0001 | c0005 | t0004 | g0212 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02896 | hp2 | a0001 | c0002 | t0015 | g0034 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02897 | hp1 | a0011 | c0014 | t0023 | g0003 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02897 | hp2 | a0001 | c0002 | t0015 | g0033 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02922 | hp1 | a0004 | c0004 | t0009 | g0265 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02922 | hp2 | a0006 | c0006 | t0032 | g0105 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02965 | hp1 | a0006 | c0006 | t0007 | g0351 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02965 | hp2 | a0001 | c0005 | t0004 | g0209 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02970 | hp1 | a0006 | c0006 | t0007 | g0333 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02970 | hp2 | a0004 | c0010 | t0009 | g0350 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03041 | hp1 | a0008 | c0009 | t0025 | g0327 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03041 | hp2 | a0001 | c0002 | t0015 | g0032 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03098 | hp1 | a0006 | c0006 | t0007 | g0357 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03098 | hp2 | a0006 | c0006 | t0007 | g0379 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03130 | hp1 | a0004 | c0010 | t0022 | g0040 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03130 | hp2 | a0004 | c0004 | t0009 | g0009 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03139 | hp1 | a0008 | c0017 | t0031 | g0109 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03139 | hp2 | a0001 | c0005 | t0029 | g0210 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03195 | hp1 | a0003 | c0003 | t0002 | g0340 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03195 | hp2 | a0008 | c0009 | t0003 | g0319 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03209 | hp1 | a0009 | c0013 | t0021 | g0126 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03209 | hp2 | a0006 | c0006 | t0007 | g0359 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03225 | hp1 | a0008 | c0009 | t0002 | g0339 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03225 | hp2 | a0004 | c0004 | t0033 | g0268 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03239 | hp1 | a0002 | c0001 | t0003 | g0219 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03239 | hp2 | a0001 | c0005 | t0005 | g0198 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03453 | hp1 | a0004 | c0004 | t0009 | g0264 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03453 | hp2 | a0006 | c0006 | t0007 | g0364 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03486 | hp1 | a0005 | c0011 | t0003 | g0336 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03486 | hp2 | a0008 | c0017 | t0013 | g0252 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0071 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03490 | hp2 | a0001 | c0005 | t0005 | g0174 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03491 | hp2 | a0017 | c0021 | t0006 | g0141 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03492 | hp1 | a0001 | c0005 | t0005 | g0175 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03492 | hp2 | a0017 | c0021 | t0006 | g0142 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03516 | hp1 | a0001 | c0005 | t0004 | g0213 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03516 | hp2 | a0006 | c0006 | t0007 | g0356 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03540 | hp1 | a0004 | c0010 | t0009 | g0349 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0131 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03579 | hp1 | a0011 | c0014 | t0035 | g0025 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03579 | hp2 | a0004 | c0010 | t0014 | g0325 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0138 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03654 | hp2 | a0004 | c0004 | t0030 | g0245 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03669 | hp1 | a0019 | c0019 | t0002 | g0288 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03669 | hp2 | a0001 | c0005 | t0005 | g0204 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0081 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0128 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03942 | hp1 | a0001 | c0002 | t0005 | g0370 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0046 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04199 | hp1 | a0004 | c0004 | t0028 | g0246 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04199 | hp2 | a0005 | c0007 | t0003 | g0181 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04204 | hp1 | a0022 | c0031 | t0001 | g0077 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04204 | hp2 | a0001 | c0005 | t0005 | g0189 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04228 | hp1 | a0004 | c0004 | t0004 | g0376 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04228 | hp2 | a0001 | c0005 | t0005 | g0186 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18522 | hp1 | a0002 | c0001 | t0003 | g0272 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18522 | hp2 | a0001 | c0005 | t0004 | g0208 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0293 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18747 | hp1 | a0004 | c0004 | t0004 | g0178 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0044 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18906 | hp1 | a0004 | c0004 | t0009 | g0258 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18906 | hp2 | a0004 | c0010 | t0014 | g0326 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18939 | hp1 | a0001 | c0002 | t0006 | g0122 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0306 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18940 | hp2 | a0005 | c0033 | t0003 | g0150 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18941 | hp1 | a0004 | c0004 | t0004 | g0229 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18941 | hp2 | a0001 | c0002 | t0008 | g0168 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18942 | hp1 | a0007 | c0008 | t0001 | g0097 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18943 | hp2 | a0001 | c0002 | t0006 | g0088 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18944 | hp2 | a0001 | c0002 | t0008 | g0171 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18945 | hp1 | a0001 | c0002 | t0008 | g0008 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18945 | hp2 | a0001 | c0002 | t0006 | g0121 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18946 | hp2 | a0005 | c0007 | t0003 | g0145 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0301 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18948 | hp2 | a0005 | c0007 | t0003 | g0147 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18949 | hp1 | a0004 | c0004 | t0004 | g0221 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0335 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18950 | hp1 | a0001 | c0002 | t0006 | g0120 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18951 | hp2 | a0003 | c0003 | t0002 | g0311 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0115 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18954 | hp2 | a0001 | c0002 | t0010 | g0166 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18956 | hp1 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18957 | hp1 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0302 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18959 | hp1 | a0004 | c0004 | t0004 | g0222 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18959 | hp2 | a0003 | c0003 | t0002 | g0010 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18960 | hp1 | a0001 | c0002 | t0008 | g0004 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0303 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18961 | hp1 | a0007 | c0008 | t0001 | g0051 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18961 | hp2 | a0003 | c0012 | t0002 | g0276 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18962 | hp1 | a0007 | c0008 | t0003 | g0148 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18965 | hp1 | a0003 | c0003 | t0002 | g0274 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18965 | hp2 | a0001 | c0002 | t0010 | g0169 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18967 | hp1 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0309 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18969 | hp2 | a0001 | c0002 | t0010 | g0005 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0085 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18972 | hp1 | a0004 | c0004 | t0004 | g0225 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18972 | hp2 | a0003 | c0012 | t0002 | g0162 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0346 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0316 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18978 | hp1 | a0015 | c0018 | t0001 | g0091 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18978 | hp2 | a0001 | c0002 | t0006 | g0084 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18980 | hp2 | a0004 | c0004 | t0004 | g0223 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18982 | hp1 | a0007 | c0008 | t0001 | g0052 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18984 | hp2 | a0007 | c0008 | t0001 | g0103 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18986 | hp1 | a0005 | c0007 | t0003 | g0149 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18986 | hp2 | a0004 | c0004 | t0004 | g0233 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18989 | hp1 | a0012 | c0016 | t0012 | g0095 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18991 | hp2 | a0003 | c0003 | t0002 | g0313 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18992 | hp1 | a0004 | c0004 | t0024 | g0241 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18992 | hp2 | a0007 | c0008 | t0001 | g0096 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18993 | hp1 | a0001 | c0002 | t0006 | g0118 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18993 | hp2 | a0005 | c0007 | t0003 | g0159 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18994 | hp1 | a0015 | c0018 | t0001 | g0089 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18994 | hp2 | a0004 | c0004 | t0004 | g0230 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18995 | hp1 | a0001 | c0002 | t0008 | g0008 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18995 | hp2 | a0003 | c0003 | t0002 | g0334 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18997 | hp1 | a0007 | c0008 | t0003 | g0238 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18997 | hp2 | a0001 | c0002 | t0008 | g0173 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0307 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18998 | hp2 | a0001 | c0002 | t0006 | g0123 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19000 | hp1 | a0005 | c0007 | t0003 | g0172 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0298 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19003 | hp1 | a0001 | c0002 | t0006 | g0116 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19003 | hp2 | a0001 | c0002 | t0010 | g0005 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19005 | hp1 | a0001 | c0002 | t0008 | g0004 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19006 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19006 | hp2 | a0001 | c0002 | t0010 | g0170 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19007 | hp1 | a0005 | c0007 | t0003 | g0152 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0304 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19009 | hp1 | a0003 | c0003 | t0002 | g0308 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19010 | hp1 | a0007 | c0008 | t0001 | g0026 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0286 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19011 | hp2 | a0001 | c0002 | t0008 | g0255 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19012 | hp1 | a0005 | c0007 | t0003 | g0163 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19012 | hp2 | a0007 | c0008 | t0001 | g0102 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19030 | hp1 | a0001 | c0002 | t0027 | g0337 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19030 | hp2 | a0006 | c0006 | t0007 | g0361 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19043 | hp1 | a0004 | c0004 | t0004 | g0250 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19043 | hp2 | a0006 | c0023 | t0007 | g0179 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19054 | hp1 | a0007 | c0008 | t0003 | g0157 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0291 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19056 | hp1 | a0004 | c0004 | t0004 | g0006 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0338 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19057 | hp2 | a0013 | c0026 | t0003 | g0235 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19058 | hp1 | a0004 | c0004 | t0004 | g0232 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0297 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19060 | hp1 | a0005 | c0007 | t0003 | g0155 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19060 | hp2 | a0003 | c0003 | t0016 | g0312 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19062 | hp1 | a0003 | c0003 | t0002 | g0300 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19062 | hp2 | a0004 | c0004 | t0004 | g0220 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19063 | hp1 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19063 | hp2 | a0001 | c0002 | t0006 | g0087 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0083 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19064 | hp2 | a0004 | c0004 | t0002 | g0228 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19065 | hp1 | a0001 | c0002 | t0006 | g0112 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19065 | hp2 | a0001 | c0002 | t0008 | g0256 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19066 | hp2 | a0005 | c0007 | t0003 | g0156 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19067 | hp1 | a0001 | c0002 | t0006 | g0107 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19067 | hp2 | a0003 | c0003 | t0002 | g0282 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0067 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19068 | hp2 | a0004 | c0004 | t0004 | g0224 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19070 | hp1 | a0005 | c0007 | t0003 | g0158 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19072 | hp1 | a0001 | c0002 | t0006 | g0137 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19072 | hp2 | a0007 | c0008 | t0001 | g0098 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19074 | hp2 | a0003 | c0003 | t0008 | g0296 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19077 | hp1 | a0001 | c0002 | t0008 | g0254 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19077 | hp2 | a0004 | c0004 | t0004 | g0226 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19079 | hp1 | a0003 | c0012 | t0012 | g0099 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19079 | hp2 | a0005 | c0007 | t0003 | g0144 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19080 | hp1 | a0004 | c0004 | t0004 | g0227 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0305 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0086 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19084 | hp2 | a0004 | c0004 | t0004 | g0146 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0278 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19085 | hp2 | a0005 | c0027 | t0003 | g0237 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19086 | hp1 | a0001 | c0030 | t0006 | g0119 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19086 | hp2 | a0004 | c0004 | t0004 | g0143 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19088 | hp1 | a0007 | c0008 | t0003 | g0153 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0281 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19090 | hp1 | a0001 | c0002 | t0006 | g0124 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0310 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19091 | hp1 | a0012 | c0016 | t0012 | g0072 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0114 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19240 | hp1 | a0001 | c0002 | t0020 | g0111 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19240 | hp2 | a0004 | c0004 | t0009 | g0261 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20129 | hp1 | a0004 | c0010 | t0014 | g0328 | AFR | ASW | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0343 | AFR | ASW | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0368 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20752 | hp2 | a0001 | c0005 | t0005 | g0001 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20805 | hp1 | a0001 | c0005 | t0005 | g0202 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20805 | hp2 | a0001 | c0005 | t0005 | g0002 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20905 | hp1 | a0004 | c0004 | t0004 | g0184 | SAS | GIH | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0140 | SAS | GIH | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02486 | hp1 | a0004 | c0004 | t0004 | g0240 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02486 | hp2 | a0008 | c0017 | t0013 | g0251 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02559 | hp1 | a0002 | c0001 | t0003 | g0218 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02559 | hp2 | a0006 | c0006 | t0034 | g0269 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03471 | hp1 | a0024 | c0037 | t0003 | g0363 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03471 | hp2 | a0008 | c0009 | t0003 | g0321 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG06807 | hp1 | a0018 | c0020 | t0017 | g0177 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0036 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20300 | hp1 | a0006 | c0006 | t0007 | g0355 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA21309 | hp1 | a0001 | c0005 | t0004 | g0211 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA21309 | hp2 | a0020 | c0032 | t0009 | g0314 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0075 | REF | REF | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| homoSapiens_grch38 | hp1 | a0023 | c0028 | t0003 | g0196 | REF | REF | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149597844
|
C | G | 1 | a0024 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.75C>G | p.Asp25Glu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/13 | 213/4943 | 75/2028 | 25/675 | chr5 | 149597844 | ||
| chr5:149609652
|
C | T | 1 | a0011 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.415C>T | p.Pro139Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 553/4943 | 415/2028 | 139/675 | chr5 | 149609652 | ||
| chr5:149609653
|
C | T | 3 | a0009a0013a0020 | 8 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
missense_variant | MODERATE | c.416C>T | p.Pro139Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 554/4943 | 416/2028 | 139/675 | chr5 | 149609653 | ||
| chr5:149616569
|
C | T | 1 | a0014 | 2 | HG00673.hp1 HG02129.hp2 |
missense_variant&splice_region_variant | MODERATE | c.461C>T | p.Pro154Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/13 | 599/4943 | 461/2028 | 154/675 | chr5 | 149616569 | ||
| chr5:149618234
|
C | A | 1 | a0015 | 2 | NA18978.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.717C>A | p.Asn239Lys | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/13 | 855/4943 | 717/2028 | 239/675 | chr5 | 149618234 | ||
| chr5:149619019
|
G | A | 1 | a0007 | 14 | HG00621.hp1 HG02074.hp1 NA18942.hp1 others(11): Show |
missense_variant | MODERATE | c.871G>A | p.Ala291Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/13 | 1009/4943 | 871/2028 | 291/675 | chr5 | 149619019 | ||
| chr5:149620422
|
C | A | 1 | a0021 | 1 | HG01169.hp1 | stop_gained | HIGH | c.963C>A | p.Cys321* | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/13 | 1101/4943 | 963/2028 | 321/675 | chr5 | 149620422 | ||
| chr5:149621790
|
C | T | 1 | a0016 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1063C>T | p.Leu355Phe | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/13 | 1201/4943 | 1063/2028 | 355/675 | chr5 | 149621790 | ||
| chr5:149621988
|
A | C | 12 | a0002a0004a0005others(9): Show | 181 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
missense_variant | MODERATE | c.1261A>C | p.Met421Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/13 | 1399/4943 | 1261/2028 | 421/675 | chr5 | 149621988 | ||
| chr5:149624027
|
G | T | 1 | a0012 | 3 | HG02027.hp1 NA18989.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.1351G>T | p.Val451Phe | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1489/4943 | 1351/2028 | 451/675 | chr5 | 149624027 | ||
| chr5:149624063
|
G | A | 1 | a0010 | 4 | HG01256.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
missense_variant | MODERATE | c.1387G>A | p.Ala463Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1525/4943 | 1387/2028 | 463/675 | chr5 | 149624063 | ||
| chr5:149624064
|
C | T | 2 | a0004a0020 | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
missense_variant | MODERATE | c.1388C>T | p.Ala463Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1526/4943 | 1388/2028 | 463/675 | chr5 | 149624064 | ||
| chr5:149627077
|
C | T | 7 | a0001a0006a0009others(4): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
missense_variant&splice_region_variant | MODERATE | c.1466C>T | p.Pro489Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1604/4943 | 1466/2028 | 489/675 | chr5 | 149627077 | ||
| chr5:149627163
|
A | C | 3 | a0004a0018a0020 | 58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
missense_variant | MODERATE | c.1552A>C | p.Ser518Arg | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1690/4943 | 1552/2028 | 518/675 | chr5 | 149627163 | ||
| chr5:149627164
|
G | T | 1 | a0019 | 2 | HG02132.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.1553G>T | p.Ser518Ile | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1691/4943 | 1553/2028 | 518/675 | chr5 | 149627164 | ||
| chr5:149628904
|
C | A | 4 | a0003a0012a0014others(1): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
missense_variant | MODERATE | c.1756C>A | p.Pro586Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1894/4943 | 1756/2028 | 586/675 | chr5 | 149628904 | ||
| chr5:149628914
|
T | C | 1 | a0022 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1766T>C | p.Leu589Pro | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1904/4943 | 1766/2028 | 589/675 | chr5 | 149628914 | ||
| chr5:149628958
|
A | G | 19 | a0001a0003a0004others(16): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
missense_variant | MODERATE | c.1810A>G | p.Met604Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1948/4943 | 1810/2028 | 604/675 | chr5 | 149628958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149609559
|
C | T | 15 | a0001c0005a0002c0024a0003c0012others(12): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
synonymous_variant | LOW | c.322C>T | p.Leu108Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 460/4943 | 322/2028 | 108/675 | chr5 | 149609559 | ||
| chr5:149616765
|
G | A | 5 | a0005c0007a0005c0027a0005c0033others(2): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
splice_region_variant&synonymous_variant | LOW | c.657G>A | p.Val219Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/13 | 795/4943 | 657/2028 | 219/675 | chr5 | 149616765 | ||
| chr5:149620377
|
C | T | 1 | a0005c0033 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.918C>T | p.His306His | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/13 | 1056/4943 | 918/2028 | 306/675 | chr5 | 149620377 | ||
| chr5:149624062
|
C | T | 1 | a0001c0030 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1386C>T | p.Asp462Asp | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1524/4943 | 1386/2028 | 462/675 | chr5 | 149624062 | ||
| chr5:149627246
|
C | T | 1 | a0003c0029 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1635C>T | p.Ser545Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1773/4943 | 1635/2028 | 545/675 | chr5 | 149627246 | ||
| chr5:149628840
|
A | G | 27 | a0001c0002a0001c0005a0001c0030others(24): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
synonymous_variant | LOW | c.1692A>G | p.Leu564Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1830/4943 | 1692/2028 | 564/675 | chr5 | 149628840 | ||
| chr5:149628921
|
G | A | 5 | a0005c0007a0005c0027a0005c0033others(2): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
synonymous_variant | LOW | c.1773G>A | p.Pro591Pro | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1911/4943 | 1773/2028 | 591/675 | chr5 | 149628921 | ||
| chr5:149632134
|
T | C | 1 | a0004c0036 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1971T>C | p.Ser657Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2109/4943 | 1971/2028 | 657/675 | chr5 | 149632134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149581555
|
C | T | 2 | a0011c0014t0023a0011c0014t0035 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-81C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | 16215 | chr5 | 149581555 | |||||
| chr5:149581558
|
C | T | 1 | a0006c0006t0034 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | chr5 | 149581558 | ||||||
| chr5:149581578
|
C | G | 20 | a0001c0002t0006a0001c0002t0015a0001c0002t0020others(17): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
5_prime_UTR_variant | MODIFIER | c.-58C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | 16192 | chr5 | 149581578 | |||||
| chr5:149632239
|
A | T | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 48 | chr5 | 149632239 | |||||
| chr5:149632372
|
G | C | 1 | a0004c0004t0024 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 181 | chr5 | 149632372 | |||||
| chr5:149632485
|
C | T | 1 | a0004c0004t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 294 | chr5 | 149632485 | |||||
| chr5:149632488
|
C | G | 25 | a0001c0002t0004a0001c0002t0005a0001c0002t0011others(22): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*297C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 297 | chr5 | 149632488 | |||||
| chr5:149632490
|
T | C | 9 | a0001c0002t0006a0001c0002t0008a0001c0002t0010others(6): Show | 58 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*299T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 299 | chr5 | 149632490 | |||||
| chr5:149632540
|
G | A | 1 | a0011c0014t0035 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*349G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 349 | chr5 | 149632540 | |||||
| chr5:149632654
|
A | G | 3 | a0004c0010t0014a0008c0017t0013a0016c0025t0013 | 7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*463A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 463 | chr5 | 149632654 | |||||
| chr5:149632896
|
G | T | 1 | a0001c0002t0010 | 5 | NA18954.hp2 NA18965.hp2 NA18969.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 705 | chr5 | 149632896 | |||||
| chr5:149632897
|
G | A | 4 | a0001c0002t0011a0009c0013t0011a0009c0013t0021others(1): Show | 7 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*706G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 706 | chr5 | 149632897 | |||||
| chr5:149632911
|
T | C | 1 | a0004c0010t0022 | 2 | HG01884.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*720T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 720 | chr5 | 149632911 | |||||
| chr5:149633044
|
C | T | 1 | a0004c0010t0022 | 2 | HG01884.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*853C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 853 | chr5 | 149633044 | |||||
| chr5:149633104
|
G | A | 1 | a0008c0009t0026 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 913 | chr5 | 149633104 | |||||
| chr5:149633219
|
G | A | 16 | a0001c0002t0004a0001c0002t0005a0001c0005t0004others(13): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1028G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1028 | chr5 | 149633219 | |||||
| chr5:149633322
|
C | T | 2 | a0008c0017t0013a0016c0025t0013 | 4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1131C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1131 | chr5 | 149633322 | |||||
| chr5:149633427
|
C | T | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1236C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1236 | chr5 | 149633427 | |||||
| chr5:149633481
|
C | A | 1 | a0004c0004t0028 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1290 | chr5 | 149633481 | |||||
| chr5:149633498
|
G | C | 2 | a0008c0017t0013a0016c0025t0013 | 4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1307 | chr5 | 149633498 | |||||
| chr5:149633644
|
C | A | 1 | a0001c0005t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1453 | chr5 | 149633644 | |||||
| chr5:149633851
|
A | G | 4 | a0006c0006t0007a0006c0006t0032a0006c0006t0034others(1): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1660A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1660 | chr5 | 149633851 | |||||
| chr5:149633998
|
A | C | 1 | a0001c0005t0019 | 2 | HG01106.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1807A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1807 | chr5 | 149633998 | |||||
| chr5:149634024
|
G | A | 12 | a0003c0003t0002a0003c0003t0012a0003c0003t0016others(9): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1833G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1833 | chr5 | 149634024 | |||||
| chr5:149634277
|
G | A | 1 | a0018c0020t0017 | 2 | HG01891.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2086G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2086 | chr5 | 149634277 | |||||
| chr5:149634281
|
T | A | 5 | a0001c0002t0005a0001c0005t0005a0001c0005t0019others(2): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2090T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2090 | chr5 | 149634281 | |||||
| chr5:149634378
|
A | T | 2 | a0001c0002t0027a0011c0014t0035 | 2 | HG03579.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2187A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2187 | chr5 | 149634378 | |||||
| chr5:149634409
|
T | C | 2 | a0008c0017t0013a0016c0025t0013 | 4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2218T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2218 | chr5 | 149634409 | |||||
| chr5:149634430
|
T | C | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2239 | chr5 | 149634430 | |||||
| chr5:149634487
|
G | C | 1 | a0008c0017t0031 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2296G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2296 | chr5 | 149634487 | |||||
| chr5:149634855
|
A | G | 19 | a0001c0002t0006a0001c0002t0008a0001c0002t0010others(16): Show | 82 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2664A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2664 | chr5 | 149634855 | |||||
| chr5:149634865
|
A | C | 2 | a0008c0017t0013a0016c0025t0013 | 4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2674A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2674 | chr5 | 149634865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149581750
|
G | T | 114 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+126G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149581750 | ||||||
| chr5:149581997
|
G | C | 11 | a0001c0002t0006g0020a0002c0001t0001g0014a0002c0001t0001g0015others(8): Show | 11 | HG01433.hp2 HG01496.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+373G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149581997 | ||||||
| chr5:149582180
|
A | G | 1 | a0006c0006t0034g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-12+556A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582180 | ||||||
| chr5:149582191
|
C | T | 1 | a0004c0004t0033g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+567C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582191 | ||||||
| chr5:149582215
|
G | A | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+591G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582215 | ||||||
| chr5:149582333
|
C | G | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+709C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582333 | ||||||
| chr5:149582346
|
G | T | 13 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+722G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582346 | ||||||
| chr5:149582459
|
C | T | 5 | a0001c0002t0008g0008a0001c0002t0008g0253a0001c0002t0008g0254others(2): Show | 6 | HG00544.hp1 NA18945.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+835C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582459 | ||||||
| chr5:149582487
|
G | T | 1 | a0006c0006t0007g0379 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+863G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582487 | ||||||
| chr5:149582498
|
C | G | 1 | a0002c0024t0003g0378 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-12+874C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582498 | ||||||
| chr5:149582668
|
T | TAAAGA | 246 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(243): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-12+1045_-12+1049d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149582668 | |||||
| chr5:149583226
|
T | C | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+1602T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583226 | ||||||
| chr5:149583229
|
C | T | 2 | a0008c0017t0013g0251a0008c0017t0013g0252 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-12+1605C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583229 | ||||||
| chr5:149583230
|
G | A | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+1606G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583230 | ||||||
| chr5:149583320
|
A | C | 14 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+1696A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583320 | ||||||
| chr5:149583411
|
C | T | 1 | a0003c0003t0002g0377 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-12+1787C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583411 | ||||||
| chr5:149583425
|
T | C | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+1801T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583425 | ||||||
| chr5:149583591
|
G | A | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+1967G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583591 | ||||||
| chr5:149583610
|
C | T | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+1986C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583610 | ||||||
| chr5:149583768
|
GT | G | 2 | a0011c0014t0023g0003a0011c0014t0035g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+2147delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149583768 | |||||
| chr5:149583823
|
C | T | 1 | a0004c0004t0004g0250 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+2199C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583823 | ||||||
| chr5:149583861
|
A | C | 2 | a0017c0021t0006g0141a0017c0021t0006g0142 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+2237A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583861 | ||||||
| chr5:149583949
|
G | A | 1 | a0007c0008t0001g0026 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12+2325G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583949 | ||||||
| chr5:149584017
|
C | T | 65 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(62): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+2393C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584017 | ||||||
| chr5:149584187
|
T | C | 2 | a0001c0005t0005g0174a0001c0005t0005g0175 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-12+2563T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584187 | ||||||
| chr5:149584364
|
AAGAG | A | 133 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(130): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-12+2748_-12+2751d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149584364 | |||||
| chr5:149584427
|
C | T | 5 | a0001c0002t0005g0374a0004c0004t0004g0013a0004c0004t0004g0373others(2): Show | 6 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2803C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584427 | ||||||
| chr5:149584428
|
G | A | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+2804G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584428 | ||||||
| chr5:149584462
|
G | A | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+2838G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584462 | ||||||
| chr5:149584648
|
C | T | 2 | a0002c0001t0001g0140a0004c0004t0004g0249 | 2 | HG00597.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-12+3024C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584648 | ||||||
| chr5:149584918
|
G | A | 13 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+3294G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584918 | ||||||
| chr5:149585159
|
C | T | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+3535C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585159 | ||||||
| chr5:149585308
|
G | A | 3 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-12+3684G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585308 | ||||||
| chr5:149585334
|
G | A | 298 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(295): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-12+3710G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585334 | ||||||
| chr5:149585435
|
C | A | 1 | a0004c0004t0004g0178 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-12+3811C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585435 | ||||||
| chr5:149585448
|
G | A | 65 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(62): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+3824G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585448 | ||||||
| chr5:149585490
|
A | G | 13 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+3866A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585490 | ||||||
| chr5:149585516
|
A | ATTAT | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+3908_-12+3911d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149585516 | |||||
| chr5:149585540
|
C | T | 50 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(47): Show | 54 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+3916C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585540 | ||||||
| chr5:149585662
|
T | A | 245 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+4038T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585662 | ||||||
| chr5:149585665
|
C | A | 245 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+4041C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585665 | ||||||
| chr5:149585674
|
C | T | 245 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+4050C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585674 | ||||||
| chr5:149585684
|
AT | A | 245 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+4066delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149585684 | |||||
| chr5:149585787
|
C | T | 1 | a0002c0001t0001g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12+4163C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585787 | ||||||
| chr5:149585849
|
G | T | 1 | a0002c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-12+4225G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585849 | ||||||
| chr5:149585902
|
C | A | 1 | a0003c0003t0002g0270 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-12+4278C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585902 | ||||||
| chr5:149585965
|
T | C | 13 | a0001c0002t0008g0317a0004c0010t0014g0325a0004c0010t0014g0326others(10): Show | 13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+4341T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585965 | ||||||
| chr5:149586001
|
C | A | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+4377C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586001 | ||||||
| chr5:149586234
|
GAAGTA | G | 115 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+4615_-12+4619d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149586234 | |||||
| chr5:149586286
|
A | T | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-12+4662A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586286 | ||||||
| chr5:149586399
|
C | T | 1 | a0001c0005t0005g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-12+4775C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586399 | ||||||
| chr5:149586442
|
CA | C | 13 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+4819delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586442 | ||||||
| chr5:149586482
|
C | T | 1 | a0004c0004t0028g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+4858C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586482 | ||||||
| chr5:149586515
|
G | A | 3 | a0003c0003t0002g0330a0003c0003t0002g0331a0003c0003t0002g0377 | 3 | HG00099.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-12+4891G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586515 | ||||||
| chr5:149586530
|
C | T | 133 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(130): Show | 134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-12+4906C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586530 | ||||||
| chr5:149586531
|
G | A | 65 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(62): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+4907G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586531 | ||||||
| chr5:149586649
|
G | A | 13 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+5025G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586649 | ||||||
| chr5:149586661
|
C | A | 2 | a0004c0004t0004g0180a0006c0023t0007g0179 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+5037C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586661 | ||||||
| chr5:149586734
|
A | G | 1 | a0004c0004t0028g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+5110A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586734 | ||||||
| chr5:149586900
|
C | T | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+5276C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586900 | ||||||
| chr5:149587043
|
G | T | 333 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(330): Show | 344 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.-12+5419G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587043 | ||||||
| chr5:149587065
|
G | A | 1 | a0002c0001t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-12+5441G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587065 | ||||||
| chr5:149587306
|
G | A | 1 | a0004c0004t0004g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-12+5682G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587306 | ||||||
| chr5:149587326
|
C | A | 1 | a0002c0001t0001g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+5702C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587326 | ||||||
| chr5:149587339
|
A | G | 122 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(119): Show | 122 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-12+5715A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587339 | ||||||
| chr5:149587403
|
A | G | 1 | a0002c0001t0003g0371 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-12+5779A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587403 | ||||||
| chr5:149587540
|
T | C | 2 | a0004c0010t0022g0040a0004c0010t0022g0041 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-12+5916T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587540 | ||||||
| chr5:149587575
|
C | T | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+5951C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587575 | ||||||
| chr5:149587689
|
C | G | 1 | a0004c0004t0004g0250 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+6065C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587689 | ||||||
| chr5:149587748
|
A | C | 1 | a0004c0004t0030g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12+6124A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587748 | ||||||
| chr5:149587887
|
C | G | 1 | a0002c0001t0001g0136 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12+6263C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587887 | ||||||
| chr5:149587894
|
C | CT | 17 | a0001c0002t0008g0173a0004c0004t0009g0009a0004c0004t0009g0257others(14): Show | 18 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12+6289dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | |||||
| chr5:149587894
|
CT | C | 154 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(151): Show | 156 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-12+6289delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | |||||
| chr5:149587894
|
CTTT | C | 112 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+6287_-12+6289d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | |||||
| chr5:149587895
|
T | C | 5 | a0001c0002t0006g0134a0001c0002t0020g0135a0002c0001t0001g0031others(2): Show | 5 | HG00609.hp2 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6271T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587895 | ||||||
| chr5:149587896
|
T | C | 124 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(121): Show | 124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-12+6272T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587896 | ||||||
| chr5:149587897
|
T | A | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+6273T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587897 | ||||||
| chr5:149587897
|
T | C | 2 | a0011c0014t0023g0003a0011c0014t0035g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+6273T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587897 | ||||||
| chr5:149587927
|
C | T | 13 | a0001c0002t0008g0317a0004c0010t0014g0325a0004c0010t0014g0326others(10): Show | 13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+6303C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587927 | ||||||
| chr5:149587939
|
C | G | 1 | a0004c0004t0004g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-12+6315C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587939 | ||||||
| chr5:149587953
|
G | A | 115 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6329G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587953 | ||||||
| chr5:149587982
|
C | T | 115 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6358C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587982 | ||||||
| chr5:149588129
|
C | T | 36 | a0003c0003t0002g0007a0004c0004t0002g0228a0004c0004t0004g0006others(33): Show | 38 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-12+6505C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588129 | ||||||
| chr5:149588133
|
G | A | 2 | a0002c0001t0001g0042a0002c0001t0001g0043 | 2 | HG00423.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-12+6509G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588133 | ||||||
| chr5:149588186
|
G | A | 115 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588186 | ||||||
| chr5:149588198
|
T | TTTTG | 121 | a0001c0002t0006g0020a0001c0002t0006g0046a0001c0002t0006g0083others(118): Show | 121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-12+6603_-12+6606d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149588198 | |||||
| chr5:149588227
|
T | C | 1 | a0003c0003t0002g0332 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-12+6603T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588227 | ||||||
| chr5:149588227
|
T | TTTGC | 114 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(111): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+6606_-12+6609d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149588227 | |||||
| chr5:149588301
|
C | A | 13 | a0001c0002t0008g0317a0004c0010t0014g0325a0004c0010t0014g0326others(10): Show | 13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+6677C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588301 | ||||||
| chr5:149588416
|
C | A | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+6792C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588416 | ||||||
| chr5:149588546
|
G | A | 1 | a0006c0006t0007g0369 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+6922G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588546 | ||||||
| chr5:149588611
|
A | G | 6 | a0001c0002t0006g0127a0001c0002t0006g0128a0001c0002t0006g0129others(3): Show | 6 | HG00738.hp2 HG01261.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+6987A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588611 | ||||||
| chr5:149588704
|
T | C | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+7080T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588704 | ||||||
| chr5:149588729
|
G | T | 246 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(243): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-12+7105G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588729 | ||||||
| chr5:149588761
|
A | G | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+7137A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588761 | ||||||
| chr5:149588808
|
G | A | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-12+7184G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588808 | ||||||
| chr5:149588812
|
G | A | 115 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+7188G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588812 | ||||||
| chr5:149588816
|
G | A | 30 | a0003c0003t0002g0007a0004c0004t0002g0228a0004c0004t0004g0006others(27): Show | 32 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12+7192G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588816 | ||||||
| chr5:149589040
|
G | A | 37 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+7416G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589040 | ||||||
| chr5:149589107
|
T | C | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+7483T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589107 | ||||||
| chr5:149589115
|
G | C | 1 | a0004c0004t0033g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+7491G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589115 | ||||||
| chr5:149589128
|
A | G | 131 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-12+7504A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589128 | ||||||
| chr5:149589194
|
TA | T | 66 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-12+7583delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149589194 | |||||
| chr5:149589323
|
T | TATTA | 129 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(126): Show | 129 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-12+7715_-12+7718d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149589323 | |||||
| chr5:149589339
|
A | T | 1 | a0004c0004t0009g0009 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+7715A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589339 | ||||||
| chr5:149589420
|
A | G | 332 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(329): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.-12+7796A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589420 | ||||||
| chr5:149589656
|
C | A | 2 | a0011c0014t0023g0003a0011c0014t0035g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+8032C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589656 | ||||||
| chr5:149589811
|
G | A | 2 | a0003c0003t0002g0334a0003c0003t0002g0335 | 2 | NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-11-7948G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589811 | ||||||
| chr5:149589853
|
G | A | 122 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(119): Show | 122 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-11-7906G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589853 | ||||||
| chr5:149590174
|
C | T | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-11-7585C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590174 | ||||||
| chr5:149590184
|
CAGAAG | C | 129 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(126): Show | 130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-7566_-11-7562d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590184 | |||||
| chr5:149590244
|
G | C | 1 | a0004c0004t0004g0373 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-11-7515G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590244 | ||||||
| chr5:149590282
|
C | CT | 159 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(156): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-11-7460dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590282 | |||||
| chr5:149590328
|
C | T | 2 | a0001c0002t0005g0367a0001c0002t0005g0368 | 2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-11-7431C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590328 | ||||||
| chr5:149590369
|
C | T | 32 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0143others(29): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-7390C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590369 | ||||||
| chr5:149590466
|
G | T | 1 | a0011c0014t0023g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-11-7293G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590466 | ||||||
| chr5:149590502
|
G | A | 4 | a0004c0004t0004g0243a0004c0004t0004g0244a0004c0004t0004g0250others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-7257G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590502 | ||||||
| chr5:149590558
|
G | A | 2 | a0011c0014t0023g0003a0011c0014t0035g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-7201G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590558 | ||||||
| chr5:149590575
|
T | A | 1 | a0011c0014t0011g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11-7184T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590575 | ||||||
| chr5:149590593
|
C | CT | 155 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(152): Show | 159 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-11-7152dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590593 | |||||
| chr5:149590701
|
T | C | 1 | a0005c0035t0003g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-11-7058T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590701 | ||||||
| chr5:149590772
|
T | C | 7 | a0001c0002t0006g0046a0001c0002t0015g0032a0001c0002t0015g0033others(4): Show | 7 | HG02280.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6987T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590772 | ||||||
| chr5:149590848
|
C | T | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-6911C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590848 | ||||||
| chr5:149590934
|
C | G | 259 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(256): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-11-6825C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590934 | ||||||
| chr5:149591063
|
G | T | 338 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(335): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.-11-6696G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591063 | ||||||
| chr5:149591160
|
C | T | 109 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-11-6599C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591160 | ||||||
| chr5:149591226
|
C | CA | 63 | a0001c0002t0005g0374a0002c0001t0003g0165a0003c0003t0002g0248others(60): Show | 65 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-11-6518dupA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | |||||
| chr5:149591226
|
CA | C | 117 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(114): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-11-6518delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | |||||
| chr5:149591226
|
CAA | C | 140 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(137): Show | 143 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-11-6519_-11-6518d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | |||||
| chr5:149591238
|
A | G | 2 | a0002c0001t0001g0104a0002c0001t0001g0139 | 2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-11-6521A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591238 | ||||||
| chr5:149591362
|
C | T | 149 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(146): Show | 153 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-11-6397C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591362 | ||||||
| chr5:149591387
|
T | A | 104 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-11-6372T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591387 | ||||||
| chr5:149591420
|
A | G | 259 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(256): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-11-6339A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591420 | ||||||
| chr5:149591681
|
A | G | 1 | a0008c0017t0013g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-6078A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591681 | ||||||
| chr5:149591742
|
A | C | 1 | a0005c0011t0001g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-11-6017A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591742 | ||||||
| chr5:149591742
|
A | G | 337 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(334): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.-11-6017A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591742 | ||||||
| chr5:149591777
|
C | A | 1 | a0002c0001t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11-5982C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591777 | ||||||
| chr5:149591782
|
T | C | 1 | a0002c0001t0001g0050 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-11-5977T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591782 | ||||||
| chr5:149591831
|
A | T | 15 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-5928A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591831 | ||||||
| chr5:149591962
|
C | T | 38 | a0001c0002t0005g0374a0003c0003t0002g0248a0004c0004t0002g0228others(35): Show | 40 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-11-5797C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591962 | ||||||
| chr5:149592062
|
C | T | 338 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(335): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.-11-5697C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592062 | ||||||
| chr5:149592100
|
A | G | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-5659A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592100 | ||||||
| chr5:149592238
|
T | A | 149 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(146): Show | 153 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-11-5521T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592238 | ||||||
| chr5:149592396
|
A | G | 2 | a0001c0005t0005g0174a0001c0005t0005g0175 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-11-5363A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592396 | ||||||
| chr5:149592577
|
A | G | 110 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-11-5182A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592577 | ||||||
| chr5:149592626
|
A | G | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-5133A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592626 | ||||||
| chr5:149592739
|
C | T | 15 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-5020C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592739 | ||||||
| chr5:149592859
|
T | C | 12 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(9): Show | 12 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-4900T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592859 | ||||||
| chr5:149593148
|
T | G | 338 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(335): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.-11-4611T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593148 | ||||||
| chr5:149593403
|
T | C | 150 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(147): Show | 154 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-11-4356T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593403 | ||||||
| chr5:149593491
|
C | T | 1 | a0014c0022t0004g0366 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-11-4268C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593491 | ||||||
| chr5:149593577
|
C | G | 149 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(146): Show | 153 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-11-4182C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593577 | ||||||
| chr5:149593678
|
T | C | 3 | a0001c0002t0027g0337a0011c0014t0023g0003a0011c0014t0035g0025 | 4 | HG02895.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-4081T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593678 | ||||||
| chr5:149593741
|
A | G | 28 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0143others(25): Show | 29 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11-4018A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593741 | ||||||
| chr5:149594008
|
G | T | 7 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(4): Show | 7 | HG02055.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-3751G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594008 | ||||||
| chr5:149594027
|
A | G | 1 | a0003c0003t0002g0313 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-11-3732A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594027 | ||||||
| chr5:149594056
|
C | T | 1 | a0002c0001t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11-3703C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594056 | ||||||
| chr5:149594394
|
C | T | 1 | a0001c0005t0004g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-3365C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594394 | ||||||
| chr5:149594566
|
T | G | 4 | a0004c0010t0022g0040a0004c0010t0022g0041a0017c0021t0006g0141others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-3193T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594566 | ||||||
| chr5:149594698
|
G | A | 130 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(127): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-11-3061G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594698 | ||||||
| chr5:149594964
|
A | G | 1 | a0007c0008t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-11-2795A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594964 | ||||||
| chr5:149595019
|
A | T | 1 | a0003c0003t0016g0312 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-11-2740A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595019 | ||||||
| chr5:149595059
|
A | T | 2 | a0001c0002t0011g0365a0003c0003t0002g0311 | 2 | HG02647.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-11-2700A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595059 | ||||||
| chr5:149595285
|
C | T | 33 | a0003c0012t0002g0161a0003c0012t0002g0162a0003c0012t0002g0164others(30): Show | 33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11-2474C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595285 | ||||||
| chr5:149595354
|
T | A | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-2405T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595354 | ||||||
| chr5:149595739
|
G | T | 5 | a0009c0013t0011g0011a0009c0013t0011g0329a0009c0013t0021g0108others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-2020G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595739 | ||||||
| chr5:149595792
|
C | T | 1 | a0006c0006t0007g0369 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-1967C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595792 | ||||||
| chr5:149595800
|
C | T | 28 | a0001c0002t0004g0352a0001c0002t0011g0365a0002c0001t0003g0272others(25): Show | 29 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-11-1959C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595800 | ||||||
| chr5:149595899
|
C | T | 1 | a0001c0002t0008g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-11-1860C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595899 | ||||||
| chr5:149595945
|
A | AT | 26 | a0002c0001t0001g0043a0004c0004t0009g0009a0004c0004t0009g0258others(23): Show | 27 | HG00423.hp2 HG00735.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-11-1799dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595945 | |||||
| chr5:149595945
|
AT | A | 71 | a0001c0002t0004g0352a0001c0002t0011g0365a0002c0001t0001g0015others(68): Show | 73 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11-1799delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595945 | |||||
| chr5:149595994
|
T | TG | 142 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(139): Show | 146 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11-1758dupG | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595994 | |||||
| chr5:149596079
|
A | G | 1 | a0003c0003t0002g0310 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-11-1680A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596079 | ||||||
| chr5:149596102
|
C | T | 143 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(140): Show | 147 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-11-1657C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596102 | ||||||
| chr5:149596118
|
A | G | 1 | a0001c0002t0006g0125 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-11-1641A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596118 | ||||||
| chr5:149596235
|
G | A | 2 | a0010c0015t0005g0182a0010c0015t0005g0183 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-11-1524G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596235 | ||||||
| chr5:149596482
|
T | G | 1 | a0003c0012t0002g0215 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11-1277T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596482 | ||||||
| chr5:149596524
|
C | T | 1 | a0005c0035t0003g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-11-1235C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596524 | ||||||
| chr5:149596594
|
C | T | 132 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(129): Show | 136 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-11-1165C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596594 | ||||||
| chr5:149596600
|
C | T | 1 | a0002c0001t0001g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-11-1159C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596600 | ||||||
| chr5:149596751
|
G | A | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11-1008G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596751 | ||||||
| chr5:149596924
|
A | T | 1 | a0004c0010t0014g0328 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11-835A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596924 | ||||||
| chr5:149596941
|
G | A | 130 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(127): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-11-818G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596941 | ||||||
| chr5:149597194
|
G | T | 1 | a0004c0004t0004g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-11-565G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597194 | ||||||
| chr5:149597235
|
A | C | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-524A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597235 | ||||||
| chr5:149597266
|
A | T | 5 | a0002c0001t0001g0090a0002c0001t0001g0092a0002c0001t0001g0093others(2): Show | 5 | NA18940.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-493A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597266 | ||||||
| chr5:149597267
|
A | T | 121 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(118): Show | 124 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-11-492A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597267 | ||||||
| chr5:149597268
|
A | T | 272 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(269): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-11-491A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597268 | ||||||
| chr5:149597269
|
A | T | 273 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.-11-490A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597269 | ||||||
| chr5:149597350
|
C | T | 1 | a0018c0020t0017g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-409C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597350 | ||||||
| chr5:149597402
|
G | C | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-357G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597402 | ||||||
| chr5:149597408
|
G | A | 70 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(67): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11-351G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597408 | ||||||
| chr5:149597478
|
C | G | 2 | a0003c0003t0002g0308a0003c0003t0002g0309 | 2 | NA18969.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-281C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597478 | ||||||
| chr5:149597588
|
T | A | 2 | a0005c0011t0003g0336a0006c0006t0032g0105 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11-171T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597588 | ||||||
| chr5:149597652
|
C | T | 6 | a0001c0002t0008g0168a0001c0002t0008g0171a0001c0002t0010g0005others(3): Show | 7 | NA18941.hp2 NA18944.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-107C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597652 | ||||||
| chr5:149597670
|
C | T | 25 | a0001c0002t0006g0045a0001c0002t0006g0046a0001c0002t0006g0084others(22): Show | 25 | HG00408.hp2 HG00738.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-89C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597670 | ||||||
| chr5:149598034
|
C | G | 1 | a0003c0012t0002g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.186+79C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598034 | ||||||
| chr5:149598050
|
C | T | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.186+95C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598050 | ||||||
| chr5:149598188
|
G | A | 3 | a0004c0010t0009g0349a0004c0010t0009g0350a0008c0009t0002g0339 | 3 | HG02970.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.186+233G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598188 | ||||||
| chr5:149598262
|
A | ACTC | 8 | a0001c0002t0005g0370a0001c0002t0006g0088a0001c0002t0008g0255others(5): Show | 8 | HG00558.hp2 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+308_186+310dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598262 | |||||
| chr5:149598263
|
C | CTCCTCT | 15 | a0001c0002t0008g0008a0001c0002t0008g0254a0001c0002t0027g0337others(12): Show | 16 | HG01496.hp2 HG01952.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.186+310_186+311ins others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCT | 28 | a0001c0002t0005g0374a0001c0005t0005g0002a0001c0005t0005g0174others(25): Show | 29 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.186+370_186+372dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCT | 22 | a0001c0005t0004g0209a0001c0005t0004g0211a0001c0005t0004g0212others(19): Show | 25 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.186+367_186+372dup others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(2): Show |
16 | a0001c0005t0004g0208a0001c0005t0005g0185a0001c0005t0005g0186others(13): Show | 18 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.186+364_186+372dup others(9): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(5): Show |
12 | a0001c0002t0011g0365a0002c0001t0003g0353a0004c0004t0004g0184others(9): Show | 12 | HG00558.hp1 HG00597.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+361_186+372dup others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(8): Show |
6 | a0003c0012t0002g0276a0004c0004t0004g0146a0005c0007t0003g0147others(3): Show | 6 | NA18940.hp2 NA18948.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+358_186+372dup others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(11): Show |
3 | a0002c0001t0003g0371a0005c0007t0003g0172a0009c0013t0021g0126 | 3 | HG00639.hp2 HG03209.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.186+355_186+372dup others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(14): Show |
1 | a0005c0007t0003g0145 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.186+352_186+372dup others(21): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
C | CTCTTCTT others(17): Show |
1 | a0005c0007t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.186+349_186+372dup others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
CTCT | C | 22 | a0001c0005t0005g0202a0001c0005t0005g0204a0001c0005t0005g0205others(19): Show | 24 | HG00673.hp2 HG00735.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+370_186+372del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
CTCTTCT | C | 12 | a0003c0003t0002g0307a0004c0004t0004g0233a0004c0004t0004g0244others(9): Show | 12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.186+367_186+372del others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
CTCTTCTT others(2): Show |
C | 7 | a0003c0012t0012g0099a0004c0004t0009g0264a0004c0004t0009g0265others(4): Show | 7 | HG00621.hp1 HG02074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+364_186+372del others(9): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
CTCTTCTT others(5): Show |
C | 5 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0267others(2): Show | 6 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+361_186+372del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598263
|
CTCTTCTT others(8): Show |
C | 3 | a0005c0007t0003g0163a0005c0011t0003g0372a0007c0008t0001g0102 | 3 | HG02615.hp2 NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.186+358_186+372del others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | |||||
| chr5:149598266
|
T | C | 114 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(111): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.186+311T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598266 | ||||||
| chr5:149598269
|
T | C | 2 | a0002c0001t0001g0030a0011c0014t0023g0003 | 3 | HG00673.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186+314T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598269 | ||||||
| chr5:149598272
|
T | C | 1 | a0004c0010t0022g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.186+317T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598272 | ||||||
| chr5:149598303
|
TCTTCTTC others(29): Show |
T | 1 | a0008c0009t0025g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186+349_186+384del others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598303 | ||||||
| chr5:149598312
|
TCTTCTTC others(20): Show |
T | 2 | a0004c0010t0014g0326a0004c0010t0014g0328 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.186+358_186+384del others(27): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598312 | ||||||
| chr5:149598322
|
CTTCT | C | 36 | a0001c0002t0005g0368a0001c0002t0006g0106a0001c0002t0006g0107others(33): Show | 38 | HG00140.hp1 HG00621.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.186+373_186+376del others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598322 | |||||
| chr5:149598323
|
TTCTTTCT others(3): Show |
T | 1 | a0001c0002t0006g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.186+373_186+382del others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598323 | |||||
| chr5:149598323
|
TTCTTTCT others(9): Show |
T | 2 | a0002c0001t0001g0068a0002c0001t0001g0069 | 2 | NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.186+373_186+388del others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598323 | |||||
| chr5:149598325
|
CT | C | 83 | a0001c0002t0005g0367a0001c0002t0006g0045a0001c0002t0006g0084others(80): Show | 84 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.186+373delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598325 | |||||
| chr5:149598326
|
T | TTC | 9 | a0001c0002t0004g0352a0003c0003t0002g0279a0003c0003t0002g0280others(6): Show | 9 | HG01074.hp1 HG01975.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+372_186+373ins others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598326 | |||||
| chr5:149598326
|
TTTCTTCC | T | 38 | a0001c0002t0006g0020a0001c0002t0006g0046a0001c0002t0006g0123others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.186+373_186+379del others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598326 | |||||
| chr5:149598327
|
TTCTTCCT others(4): Show |
T | 1 | a0005c0027t0003g0237 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.186+373_186+383del others(11): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598327 | ||||||
| chr5:149598333
|
C | T | 129 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(126): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.186+378C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598333 | ||||||
| chr5:149598337
|
TCC | T | 31 | a0001c0002t0005g0368a0002c0001t0003g0295a0003c0003t0002g0012others(28): Show | 32 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+383_186+384del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598337 | ||||||
| chr5:149598338
|
C | CT | 25 | a0001c0002t0005g0367a0003c0003t0002g0279a0003c0003t0002g0280others(22): Show | 25 | HG00438.hp1 HG01074.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.186+383_186+384ins others(1): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598338 | ||||||
| chr5:149598339
|
C | T | 135 | a0001c0002t0005g0367a0001c0002t0006g0020a0001c0002t0006g0045others(132): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.186+384C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598339 | ||||||
| chr5:149598343
|
TCC | T | 71 | a0001c0002t0006g0020a0001c0002t0006g0046a0001c0002t0006g0086others(68): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.186+389_186+390del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598343 | ||||||
| chr5:149598344
|
C | CT | 4 | a0003c0003t0002g0277a0004c0004t0004g0222a0004c0004t0004g0373others(1): Show | 4 | HG00280.hp2 HG01952.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+389_186+390ins others(1): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598344 | ||||||
| chr5:149598344
|
CCTCTT | C | 16 | a0001c0002t0006g0045a0001c0002t0006g0084a0001c0002t0006g0085others(13): Show | 16 | HG00323.hp1 HG01099.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+392_186+396del others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598344 | |||||
| chr5:149598345
|
C | T | 24 | a0001c0002t0006g0112a0001c0002t0006g0113a0001c0002t0006g0114others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.186+390C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598345 | ||||||
| chr5:149598348
|
TTC | T | 6 | a0001c0002t0006g0114a0001c0002t0006g0115a0001c0002t0006g0116others(3): Show | 6 | HG01943.hp1 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+395_186+396del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | |||||
| chr5:149598348
|
TTCTTCTT others(8): Show |
T | 65 | a0001c0002t0005g0374a0003c0003t0002g0007a0003c0003t0002g0010others(62): Show | 70 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.186+427_186+441del others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | |||||
| chr5:149598348
|
TTCTTCTT others(23): Show |
T | 31 | a0001c0002t0005g0370a0001c0002t0006g0083a0001c0002t0006g0088others(28): Show | 33 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.186+412_186+441del others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | |||||
| chr5:149598350
|
C | CT | 6 | a0001c0002t0006g0113a0002c0001t0001g0042a0002c0001t0001g0049others(3): Show | 6 | HG00140.hp2 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+397dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598350 | |||||
| chr5:149598350
|
C | T | 16 | a0001c0002t0006g0045a0001c0002t0006g0084a0001c0002t0006g0085others(13): Show | 16 | HG00323.hp1 HG01099.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+395C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598350 | ||||||
| chr5:149598351
|
T | C | 138 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0006g0020others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.186+396T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598351 | ||||||
| chr5:149598355
|
TCC | T | 3 | a0002c0001t0001g0036a0002c0001t0001g0068a0002c0001t0001g0069 | 3 | HG06807.hp2 NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.186+401_186+402del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598355 | ||||||
| chr5:149598357
|
C | T | 2 | a0002c0001t0001g0139a0005c0011t0003g0336 | 2 | HG03486.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.186+402C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598357 | ||||||
| chr5:149598360
|
TTCC | T | 61 | a0001c0002t0005g0367a0001c0002t0005g0368a0002c0001t0003g0295others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.186+408_186+410del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598360 | |||||
| chr5:149598363
|
C | CTCT | 4 | a0003c0003t0002g0277a0004c0004t0004g0222a0004c0004t0004g0373others(1): Show | 4 | HG00280.hp2 HG01952.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+414_186+416dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598363 | |||||
| chr5:149598363
|
CTCT | C | 35 | a0001c0002t0006g0045a0001c0002t0006g0084a0001c0002t0006g0085others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.186+414_186+416del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598363 | |||||
| chr5:149598366
|
TTCTTCCT others(5): Show |
T | 71 | a0001c0002t0006g0020a0001c0002t0006g0046a0001c0002t0006g0086others(68): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.186+417_186+428del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598366 | |||||
| chr5:149598369
|
T | C | 2 | a0002c0001t0001g0036a0002c0001t0001g0139 | 2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+414T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598369 | ||||||
| chr5:149598372
|
C | T | 2 | a0002c0001t0001g0036a0002c0001t0001g0139 | 2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+417C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598372 | ||||||
| chr5:149598375
|
T | C | 2 | a0002c0001t0001g0036a0002c0001t0001g0139 | 2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+420T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598375 | ||||||
| chr5:149598375
|
TTCC | T | 32 | a0001c0002t0006g0045a0001c0002t0006g0084a0001c0002t0006g0085others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+423_186+425del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598375 | |||||
| chr5:149598378
|
C | T | 2 | a0002c0001t0001g0036a0002c0001t0001g0139 | 2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+423C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598378 | ||||||
| chr5:149598439
|
CCTTCCTC others(12): Show |
C | 5 | a0002c0001t0001g0133a0002c0001t0003g0216a0002c0001t0003g0217others(2): Show | 5 | HG00323.hp1 HG00741.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+486_186+504del others(19): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598439 | |||||
| chr5:149598542
|
T | C | 141 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(138): Show | 145 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.186+587T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598542 | ||||||
| chr5:149598544
|
A | G | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.186+589A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598544 | ||||||
| chr5:149598554
|
T | C | 1 | a0004c0010t0014g0325 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186+599T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598554 | ||||||
| chr5:149598560
|
C | A | 1 | a0011c0014t0023g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186+605C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598560 | ||||||
| chr5:149598737
|
C | CAT | 4 | a0001c0002t0027g0337a0011c0014t0011g0275a0011c0014t0023g0003others(1): Show | 5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+793_186+794dup others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598737 | |||||
| chr5:149598744
|
A | C | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.186+789A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598744 | ||||||
| chr5:149598745
|
TATATCTA others(7): Show |
T | 5 | a0002c0001t0001g0017a0002c0001t0001g0047a0002c0001t0001g0061others(2): Show | 5 | NA18946.hp1 NA18967.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+795_186+808del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598745 | |||||
| chr5:149598747
|
TATCTATA others(5): Show |
T | 116 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(113): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.186+795_186+806del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | |||||
| chr5:149598747
|
TATCTATA others(11): Show |
T | 2 | a0004c0004t0004g0229a0004c0004t0004g0230 | 2 | NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.186+795_186+812del others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | |||||
| chr5:149598747
|
TATCTATA others(17): Show |
T | 1 | a0019c0019t0002g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186+795_186+818del others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | |||||
| chr5:149598748
|
ATC | A | 116 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(113): Show | 119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.186+795_186+796del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598748 | |||||
| chr5:149598750
|
C | A | 29 | a0001c0002t0006g0083a0001c0002t0015g0032a0001c0002t0020g0135others(26): Show | 30 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.186+795C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598750 | ||||||
| chr5:149598753
|
T | TATATAGA others(5): Show |
1 | a0005c0007t0003g0172 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.186+816_186+827dup others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598753 | |||||
| chr5:149598753
|
TATATAG | T | 5 | a0001c0005t0005g0174a0001c0005t0005g0175a0002c0001t0003g0272others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+822_186+827del others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598753 | |||||
| chr5:149598757
|
TAGATATA others(7): Show |
T | 6 | a0002c0001t0001g0036a0002c0001t0001g0055a0002c0001t0001g0060others(3): Show | 6 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+804_186+817del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598757 | |||||
| chr5:149598759
|
G | T | 13 | a0001c0002t0015g0033a0001c0002t0015g0034a0004c0010t0014g0325others(10): Show | 13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.186+804G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598759 | ||||||
| chr5:149598759
|
GATATAGA others(13): Show |
G | 1 | a0001c0002t0008g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.186+822_186+841del others(20): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598759 | |||||
| chr5:149598761
|
T | G | 116 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(113): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.186+806T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598761 | ||||||
| chr5:149598761
|
T | TATATATA others(17): Show |
1 | a0008c0009t0003g0323 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(21): Show |
1 | a0004c0010t0014g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(28): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(19): Show |
1 | a0008c0009t0003g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(23): Show |
1 | a0004c0010t0014g0325 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(27): Show |
1 | a0004c0010t0014g0328 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(21): Show |
1 | a0008c0009t0003g0322 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(28): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(23): Show |
1 | a0008c0009t0025g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(27): Show |
1 | a0008c0009t0003g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(25): Show |
1 | a0005c0011t0003g0324 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(32): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598761
|
T | TATATATA others(29): Show |
2 | a0008c0009t0003g0320a0008c0009t0026g0318 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.186+809_186+810ins others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | |||||
| chr5:149598763
|
T | C | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.186+808T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598763 | ||||||
| chr5:149598765
|
GATATAGA others(7): Show |
G | 111 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(108): Show | 114 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.186+836_186+849del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598765 | |||||
| chr5:149598767
|
T | G | 2 | a0004c0004t0004g0229a0004c0004t0004g0230 | 2 | NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.186+812T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598767 | ||||||
| chr5:149598773
|
T | G | 1 | a0019c0019t0002g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186+818T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598773 | ||||||
| chr5:149598777
|
GAT | G | 14 | a0001c0002t0015g0033a0001c0002t0015g0034a0002c0001t0001g0017others(11): Show | 14 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+828_186+829del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598777 | |||||
| chr5:149598779
|
T | G | 8 | a0005c0011t0003g0324a0008c0009t0003g0319a0008c0009t0003g0320others(5): Show | 8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+824T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598779 | ||||||
| chr5:149598785
|
GATATAGA others(9): Show |
G | 1 | a0001c0002t0005g0370 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186+836_186+851del others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598785 | |||||
| chr5:149598787
|
TATAGATA others(5): Show |
T | 1 | a0001c0002t0020g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.186+836_186+847del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598787 | |||||
| chr5:149598808
|
A | G | 1 | a0001c0002t0020g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.186+853A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598808 | ||||||
| chr5:149598808
|
ATG | A | 38 | a0001c0005t0019g0195a0003c0012t0002g0161a0003c0012t0002g0162others(35): Show | 38 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.186+867_186+868del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598808 | |||||
| chr5:149598810
|
G | A | 1 | a0001c0002t0005g0370 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186+855G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598810 | ||||||
| chr5:149598822
|
G | A | 197 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(194): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.186+867G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598822 | ||||||
| chr5:149598867
|
T | G | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+912T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598867 | ||||||
| chr5:149598959
|
G | A | 1 | a0001c0005t0005g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.186+1004G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598959 | ||||||
| chr5:149599290
|
A | T | 1 | a0002c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.186+1335A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599290 | ||||||
| chr5:149599299
|
C | T | 7 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(4): Show | 7 | HG02055.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+1344C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599299 | ||||||
| chr5:149599314
|
G | A | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.186+1359G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599314 | ||||||
| chr5:149599434
|
C | CTTACTTA others(17): Show |
7 | a0005c0011t0003g0324a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+1482_186+1483i others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTACTTA others(21): Show |
3 | a0004c0010t0014g0325a0004c0010t0014g0326a0008c0009t0003g0319 | 3 | HG03195.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186+1482_186+1483i others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTACTTA others(25): Show |
1 | a0004c0010t0014g0328 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186+1482_186+1483i others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(1): Show |
3 | a0001c0002t0006g0046a0001c0002t0006g0106a0004c0004t0004g0220 | 3 | HG00738.hp1 HG03942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.186+1495_186+1502d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(5): Show |
11 | a0002c0001t0001g0056a0002c0001t0001g0075a0002c0001t0001g0076others(8): Show | 11 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+1491_186+1502d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(9): Show |
1 | a0003c0003t0002g0284 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.186+1487_186+1502d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(13): Show |
162 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(159): Show | 167 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.186+1483_186+1502d others(22): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(17): Show |
81 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0006g0083others(78): Show | 84 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(21): Show |
20 | a0001c0002t0015g0033a0001c0002t0015g0034a0003c0003t0002g0285others(17): Show | 20 | HG00140.hp1 HG00735.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(25): Show |
39 | a0001c0002t0005g0374a0001c0002t0011g0365a0003c0003t0002g0012others(36): Show | 40 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(29): Show |
7 | a0001c0002t0005g0368a0002c0001t0003g0295a0003c0003t0002g0007others(4): Show | 9 | HG00423.hp1 HG01081.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(38): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599434
|
C | CTTATTTA others(33): Show |
3 | a0003c0003t0002g0303a0003c0003t0002g0307a0003c0003t0008g0296 | 3 | NA18960.hp2 NA18998.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.186+1502_186+1503i others(42): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | |||||
| chr5:149599702
|
A | T | 1 | a0004c0004t0004g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1406A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599702 | ||||||
| chr5:149599864
|
T | A | 6 | a0001c0002t0006g0084a0001c0002t0006g0117a0001c0002t0006g0124others(3): Show | 6 | HG00408.hp2 HG02129.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1244T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599864 | ||||||
| chr5:149600097
|
A | G | 375 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(372): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.187-1011A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600097 | ||||||
| chr5:149600214
|
A | G | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187-894A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600214 | ||||||
| chr5:149600265
|
C | T | 2 | a0004c0004t0004g0240a0004c0004t0030g0245 | 2 | HG02486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.187-843C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600265 | ||||||
| chr5:149600350
|
G | A | 12 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(9): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.187-758G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600350 | ||||||
| chr5:149600546
|
G | A | 1 | a0005c0011t0003g0324 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.187-562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600546 | ||||||
| chr5:149600585
|
T | C | 338 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(335): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.187-523T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600585 | ||||||
| chr5:149600597
|
A | C | 1 | a0001c0005t0005g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.187-511A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600597 | ||||||
| chr5:149600604
|
C | T | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187-504C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600604 | ||||||
| chr5:149600605
|
G | A | 48 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(45): Show | 51 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.187-503G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600605 | ||||||
| chr5:149600644
|
A | AT | 234 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(231): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.187-450dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149600644 | |||||
| chr5:149600644
|
A | ATT | 13 | a0003c0003t0002g0301a0003c0003t0002g0302a0003c0003t0002g0335others(10): Show | 14 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.187-451_187-450dup others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149600644 | |||||
| chr5:149600738
|
T | A | 2 | a0003c0003t0002g0340a0003c0003t0002g0343 | 2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.187-370T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600738 | ||||||
| chr5:149600768
|
T | C | 2 | a0013c0026t0003g0234a0013c0026t0003g0235 | 2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.187-340T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600768 | ||||||
| chr5:149600799
|
C | T | 14 | a0001c0002t0008g0004a0001c0002t0008g0008a0001c0002t0008g0167others(11): Show | 17 | HG00544.hp1 HG02040.hp1 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.187-309C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600799 | ||||||
| chr5:149600803
|
C | A | 2 | a0013c0026t0003g0234a0013c0026t0003g0235 | 2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.187-305C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600803 | ||||||
| chr5:149600805
|
A | G | 1 | a0004c0004t0004g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.187-303A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600805 | ||||||
| chr5:149600889
|
A | G | 336 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(333): Show | 347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.187-219A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600889 | ||||||
| chr5:149601048
|
C | T | 3 | a0004c0004t0004g0222a0004c0004t0004g0223a0004c0004t0004g0224 | 3 | NA18959.hp1 NA18980.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.187-60C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149601048 | ||||||
| chr5:149601253
|
T | C | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.310+22T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601253 | ||||||
| chr5:149601265
|
G | A | 9 | a0004c0004t0004g0013a0004c0004t0004g0243a0004c0004t0004g0244others(6): Show | 10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.310+34G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601265 | ||||||
| chr5:149601265
|
G | C | 1 | a0001c0002t0027g0337 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.310+34G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601265 | ||||||
| chr5:149601317
|
G | C | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.310+86G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601317 | ||||||
| chr5:149601466
|
A | G | 130 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(127): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.310+235A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601466 | ||||||
| chr5:149601471
|
C | T | 1 | a0002c0001t0001g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.310+240C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601471 | ||||||
| chr5:149601483
|
T | C | 273 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.310+252T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601483 | ||||||
| chr5:149601533
|
C | T | 2 | a0016c0025t0013g0262a0016c0025t0013g0263 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.310+302C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601533 | ||||||
| chr5:149601564
|
G | C | 1 | a0003c0003t0002g0347 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.310+333G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601564 | ||||||
| chr5:149601606
|
G | A | 1 | a0002c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.310+375G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601606 | ||||||
| chr5:149601645
|
A | G | 2 | a0013c0026t0003g0234a0013c0026t0003g0235 | 2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.310+414A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601645 | ||||||
| chr5:149601704
|
G | A | 35 | a0003c0012t0002g0161a0003c0012t0002g0162a0003c0012t0002g0164others(32): Show | 35 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.310+473G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601704 | ||||||
| chr5:149601859
|
G | A | 2 | a0005c0007t0003g0158a0005c0007t0003g0172 | 2 | NA19000.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.310+628G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601859 | ||||||
| chr5:149601902
|
T | C | 1 | a0001c0005t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.310+671T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601902 | ||||||
| chr5:149602031
|
C | T | 1 | a0003c0003t0002g0274 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.310+800C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602031 | ||||||
| chr5:149602059
|
CTT | C | 255 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(252): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.310+842_310+843del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602059 | |||||
| chr5:149602143
|
G | A | 1 | a0002c0001t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.310+912G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602143 | ||||||
| chr5:149602182
|
G | A | 140 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(137): Show | 144 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.310+951G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602182 | ||||||
| chr5:149602202
|
G | A | 1 | a0006c0006t0007g0379 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310+971G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602202 | ||||||
| chr5:149602205
|
C | T | 18 | a0001c0002t0004g0352a0001c0002t0011g0365a0005c0011t0003g0372others(15): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.310+974C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602205 | ||||||
| chr5:149602257
|
G | A | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.310+1026G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602257 | ||||||
| chr5:149602262
|
G | T | 1 | a0001c0005t0005g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.310+1031G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602262 | ||||||
| chr5:149602492
|
A | AT | 48 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(45): Show | 51 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.310+1274dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602492 | |||||
| chr5:149602492
|
AT | A | 138 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(135): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.310+1274delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602492 | |||||
| chr5:149602534
|
C | A | 1 | a0005c0035t0003g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.310+1303C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602534 | ||||||
| chr5:149602621
|
A | C | 1 | a0005c0007t0003g0149 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.310+1390A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602621 | ||||||
| chr5:149602721
|
G | A | 29 | a0001c0002t0004g0352a0001c0002t0011g0365a0002c0001t0003g0272others(26): Show | 30 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.310+1490G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602721 | ||||||
| chr5:149602798
|
A | T | 138 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(135): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.310+1567A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602798 | ||||||
| chr5:149602800
|
T | A | 18 | a0001c0002t0004g0352a0001c0002t0011g0365a0005c0011t0003g0372others(15): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.310+1569T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602800 | ||||||
| chr5:149602982
|
G | A | 1 | a0003c0003t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.310+1751G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602982 | ||||||
| chr5:149602987
|
C | T | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.310+1756C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602987 | ||||||
| chr5:149602988
|
G | A | 3 | a0005c0011t0003g0336a0006c0006t0032g0105a0008c0017t0031g0109 | 3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.310+1757G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602988 | ||||||
| chr5:149603036
|
G | A | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+1805G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603036 | ||||||
| chr5:149603051
|
A | G | 339 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(336): Show | 350 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.310+1820A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603051 | ||||||
| chr5:149603114
|
G | A | 4 | a0001c0002t0027g0337a0011c0014t0011g0275a0011c0014t0023g0003others(1): Show | 5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+1883G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603114 | ||||||
| chr5:149603142
|
A | G | 131 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(128): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.310+1911A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603142 | ||||||
| chr5:149603222
|
C | T | 3 | a0005c0011t0003g0336a0006c0006t0032g0105a0008c0017t0031g0109 | 3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.310+1991C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603222 | ||||||
| chr5:149603692
|
T | G | 126 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(123): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.310+2461T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603692 | ||||||
| chr5:149603725
|
C | T | 1 | a0001c0005t0005g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.310+2494C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603725 | ||||||
| chr5:149603872
|
G | T | 2 | a0008c0009t0003g0319a0008c0009t0003g0320 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310+2641G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603872 | ||||||
| chr5:149604082
|
G | A | 1 | a0003c0003t0002g0281 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.310+2851G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604082 | ||||||
| chr5:149604239
|
C | T | 1 | a0008c0009t0025g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310+3008C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604239 | ||||||
| chr5:149604438
|
C | A | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.310+3207C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604438 | ||||||
| chr5:149604556
|
A | C | 2 | a0013c0026t0003g0234a0013c0026t0003g0235 | 2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.310+3325A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604556 | ||||||
| chr5:149604603
|
C | T | 1 | a0002c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+3372C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604603 | ||||||
| chr5:149604676
|
A | AT | 27 | a0001c0002t0004g0352a0001c0002t0011g0365a0001c0005t0004g0208others(24): Show | 28 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.310+3469dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | |||||
| chr5:149604676
|
A | ATT | 7 | a0001c0005t0004g0213a0001c0005t0004g0214a0004c0004t0033g0268others(4): Show | 7 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+3468_310+3469d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | |||||
| chr5:149604676
|
AT | A | 71 | a0001c0002t0006g0045a0001c0002t0006g0046a0001c0002t0006g0084others(68): Show | 71 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.310+3469delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | |||||
| chr5:149604676
|
ATT | A | 185 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(182): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.310+3468_310+3469d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | |||||
| chr5:149604676
|
ATTT | A | 51 | a0001c0002t0027g0337a0002c0001t0001g0058a0002c0001t0001g0074others(48): Show | 53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.310+3467_310+3469d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | |||||
| chr5:149604708
|
AATCT | A | 138 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(135): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.310+3478_310+3481d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604708 | ||||||
| chr5:149604709
|
ATCTC | A | 133 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.310+3484_310+3487d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604709 | |||||
| chr5:149604713
|
C | T | 138 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(135): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.310+3482C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604713 | ||||||
| chr5:149604785
|
C | T | 138 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(135): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.310+3554C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604785 | ||||||
| chr5:149604828
|
G | A | 1 | a0002c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+3597G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604828 | ||||||
| chr5:149604832
|
G | A | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+3601G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604832 | ||||||
| chr5:149604844
|
G | A | 7 | a0001c0002t0006g0045a0001c0002t0006g0123a0009c0013t0011g0011others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.310+3613G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604844 | ||||||
| chr5:149604891
|
C | T | 3 | a0001c0005t0005g0187a0001c0005t0005g0197a0004c0004t0004g0184 | 3 | HG00280.hp1 HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.310+3660C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604891 | ||||||
| chr5:149604965
|
G | A | 1 | a0003c0003t0016g0312 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.310+3734G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604965 | ||||||
| chr5:149605078
|
T | G | 1 | a0003c0003t0002g0270 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+3847T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605078 | ||||||
| chr5:149605169
|
G | A | 1 | a0003c0003t0002g0270 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+3938G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605169 | ||||||
| chr5:149605196
|
C | A | 1 | a0003c0003t0002g0281 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.310+3965C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605196 | ||||||
| chr5:149605226
|
CA | C | 211 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(208): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.310+4010delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149605226 | |||||
| chr5:149605301
|
A | G | 272 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(269): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.310+4070A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605301 | ||||||
| chr5:149605461
|
G | A | 1 | a0002c0001t0001g0069 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.311-4087G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605461 | ||||||
| chr5:149605505
|
T | C | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.311-4043T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605505 | ||||||
| chr5:149605511
|
C | T | 3 | a0005c0011t0003g0336a0006c0006t0032g0105a0008c0017t0031g0109 | 3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.311-4037C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605511 | ||||||
| chr5:149605885
|
T | C | 4 | a0004c0004t0009g0258a0004c0004t0009g0259a0004c0004t0009g0260others(1): Show | 4 | HG02717.hp1 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-3663T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605885 | ||||||
| chr5:149605986
|
G | A | 1 | a0002c0001t0001g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.311-3562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605986 | ||||||
| chr5:149606197
|
C | T | 1 | a0003c0003t0002g0300 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.311-3351C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606197 | ||||||
| chr5:149606228
|
C | T | 40 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(37): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-3320C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606228 | ||||||
| chr5:149606298
|
T | TG | 3 | a0005c0011t0003g0336a0006c0006t0032g0105a0008c0017t0031g0109 | 3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.311-3249dupG | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149606298 | |||||
| chr5:149606381
|
C | T | 2 | a0003c0003t0002g0315a0003c0003t0002g0316 | 2 | HG00438.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.311-3167C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606381 | ||||||
| chr5:149606436
|
G | A | 271 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(268): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.311-3112G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606436 | ||||||
| chr5:149606462
|
T | A | 69 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(66): Show | 72 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.311-3086T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606462 | ||||||
| chr5:149606518
|
C | T | 7 | a0002c0001t0001g0035a0002c0001t0001g0057a0002c0001t0001g0058others(4): Show | 7 | HG01099.hp1 HG01255.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-3030C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606518 | ||||||
| chr5:149606681
|
G | C | 149 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(146): Show | 153 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.311-2867G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606681 | ||||||
| chr5:149606781
|
G | A | 5 | a0009c0013t0011g0011a0009c0013t0011g0329a0009c0013t0021g0108others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-2767G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606781 | ||||||
| chr5:149606813
|
C | G | 40 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(37): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-2735C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606813 | ||||||
| chr5:149606980
|
A | G | 80 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(77): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.311-2568A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606980 | ||||||
| chr5:149607017
|
G | A | 1 | a0002c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.311-2531G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607017 | ||||||
| chr5:149607365
|
T | C | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-2183T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607365 | ||||||
| chr5:149607455
|
A | C | 9 | a0004c0004t0004g0013a0004c0004t0004g0243a0004c0004t0004g0244others(6): Show | 10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.311-2093A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607455 | ||||||
| chr5:149607505
|
A | G | 3 | a0011c0014t0011g0275a0011c0014t0023g0003a0011c0014t0035g0025 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2043A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607505 | ||||||
| chr5:149607755
|
C | CT | 20 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0128others(17): Show | 20 | HG01175.hp2 HG01358.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.311-1768dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | |||||
| chr5:149607755
|
CT | C | 67 | a0001c0002t0006g0129a0001c0002t0006g0137a0002c0001t0001g0047others(64): Show | 70 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.311-1768delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | |||||
| chr5:149607755
|
CTTTT | C | 34 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(31): Show | 37 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1771_311-1768d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | |||||
| chr5:149607755
|
CTTTTTTT others(3): Show |
C | 37 | a0003c0012t0002g0161a0003c0012t0002g0162a0003c0012t0002g0164others(34): Show | 37 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1777_311-1768d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | |||||
| chr5:149607755
|
CTTTTTTT others(6): Show |
C | 1 | a0009c0013t0011g0011 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.311-1780_311-1768d others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | |||||
| chr5:149607890
|
C | T | 40 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(37): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-1658C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607890 | ||||||
| chr5:149607958
|
C | T | 69 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0374others(66): Show | 72 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.311-1590C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607958 | ||||||
| chr5:149607976
|
G | A | 3 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.311-1572G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607976 | ||||||
| chr5:149608262
|
CTGACATA others(27): Show |
C | 368 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(365): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.311-1243_311-1210d others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149608262 | |||||
| chr5:149608376
|
T | A | 77 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(74): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.311-1172T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608376 | ||||||
| chr5:149608377
|
T | A | 1 | a0007c0008t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.311-1171T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608377 | ||||||
| chr5:149608397
|
G | A | 2 | a0017c0021t0006g0141a0017c0021t0006g0142 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.311-1151G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608397 | ||||||
| chr5:149608402
|
G | C | 1 | a0006c0006t0007g0361 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.311-1146G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608402 | ||||||
| chr5:149608537
|
T | A | 40 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(37): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-1011T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608537 | ||||||
| chr5:149608560
|
G | A | 78 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(75): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.311-988G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608560 | ||||||
| chr5:149608665
|
C | T | 1 | a0001c0002t0006g0124 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.311-883C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608665 | ||||||
| chr5:149609108
|
T | C | 1 | a0004c0004t0009g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.311-440T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609108 | ||||||
| chr5:149609161
|
G | A | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.311-387G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609161 | ||||||
| chr5:149609168
|
G | C | 2 | a0001c0002t0015g0033a0001c0002t0015g0034 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.311-380G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609168 | ||||||
| chr5:149609205
|
A | AAAACAAA others(1): Show |
37 | a0003c0012t0002g0161a0003c0012t0002g0162a0003c0012t0002g0164others(34): Show | 37 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-337_311-336ins others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149609205 | |||||
| chr5:149609208
|
A | G | 11 | a0001c0002t0006g0083a0002c0001t0001g0036a0002c0001t0001g0044others(8): Show | 11 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-340A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609208 | ||||||
| chr5:149609237
|
A | G | 1 | a0002c0024t0003g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.311-311A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609237 | ||||||
| chr5:149609260
|
G | A | 207 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(204): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.311-288G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609260 | ||||||
| chr5:149609366
|
C | T | 4 | a0001c0002t0010g0005a0001c0002t0010g0166a0001c0002t0010g0169others(1): Show | 5 | NA18954.hp2 NA18965.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-182C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609366 | ||||||
| chr5:149609370
|
T | C | 2 | a0002c0001t0001g0140a0022c0031t0001g0077 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.311-178T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609370 | ||||||
| chr5:149609414
|
G | T | 2 | a0006c0006t0007g0364a0024c0037t0003g0363 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.311-134G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609414 | ||||||
| chr5:149609534
|
G | A | 5 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034others(2): Show | 5 | HG00423.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-14G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609534 | ||||||
| chr5:149609740
|
C | T | 12 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(9): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.458+45C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609740 | ||||||
| chr5:149609749
|
A | G | 129 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(126): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+54A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609749 | ||||||
| chr5:149609757
|
T | C | 129 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(126): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+62T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609757 | ||||||
| chr5:149609795
|
C | T | 51 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(48): Show | 54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.458+100C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609795 | ||||||
| chr5:149609844
|
G | A | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.458+149G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609844 | ||||||
| chr5:149609847
|
A | G | 311 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(308): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.458+152A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609847 | ||||||
| chr5:149609847
|
A | T | 51 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(48): Show | 54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.458+152A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609847 | ||||||
| chr5:149609999
|
AGTAACTG others(10): Show |
A | 1 | a0001c0002t0008g0173 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.458+305_458+321del others(17): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609999 | ||||||
| chr5:149610000
|
G | A | 2 | a0002c0001t0001g0104a0002c0001t0001g0139 | 2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.458+305G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610000 | ||||||
| chr5:149610034
|
G | A | 11 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.458+339G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610034 | ||||||
| chr5:149610087
|
C | T | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.458+392C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610087 | ||||||
| chr5:149610164
|
A | G | 1 | a0007c0008t0001g0102 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.458+469A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610164 | ||||||
| chr5:149610178
|
G | A | 129 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(126): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+483G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610178 | ||||||
| chr5:149610183
|
C | G | 126 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(123): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.458+488C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610183 | ||||||
| chr5:149610325
|
G | A | 1 | a0002c0001t0001g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.458+630G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610325 | ||||||
| chr5:149610396
|
A | G | 2 | a0013c0026t0003g0234a0013c0026t0003g0235 | 2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.458+701A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610396 | ||||||
| chr5:149610418
|
C | T | 3 | a0003c0012t0002g0276a0005c0007t0003g0144a0005c0007t0003g0159 | 3 | NA18961.hp2 NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.458+723C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610418 | ||||||
| chr5:149610444
|
G | A | 128 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(125): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.458+749G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610444 | ||||||
| chr5:149610630
|
G | A | 27 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0143others(24): Show | 28 | HG00438.hp1 HG00597.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.458+935G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610630 | ||||||
| chr5:149610650
|
T | G | 40 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(37): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.458+955T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610650 | ||||||
| chr5:149610869
|
C | T | 4 | a0001c0002t0027g0337a0011c0014t0011g0275a0011c0014t0023g0003others(1): Show | 5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+1174C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610869 | ||||||
| chr5:149611087
|
G | A | 1 | a0001c0005t0005g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458+1392G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611087 | ||||||
| chr5:149611207
|
C | T | 1 | a0008c0009t0025g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458+1512C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611207 | ||||||
| chr5:149611301
|
A | T | 2 | a0017c0021t0006g0141a0017c0021t0006g0142 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.458+1606A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611301 | ||||||
| chr5:149611307
|
G | T | 361 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(358): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.458+1612G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611307 | ||||||
| chr5:149611443
|
C | T | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458+1748C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611443 | ||||||
| chr5:149611496
|
A | G | 1 | a0001c0002t0006g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.458+1801A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611496 | ||||||
| chr5:149611598
|
G | A | 1 | a0002c0001t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.458+1903G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611598 | ||||||
| chr5:149611802
|
C | T | 131 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(128): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.458+2107C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611802 | ||||||
| chr5:149611927
|
G | T | 129 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(126): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+2232G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611927 | ||||||
| chr5:149612177
|
C | CT | 42 | a0001c0005t0004g0208a0001c0005t0004g0209a0001c0005t0004g0211others(39): Show | 45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.458+2490dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149612177 | |||||
| chr5:149612190
|
T | C | 2 | a0005c0011t0003g0336a0006c0006t0032g0105 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.458+2495T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612190 | ||||||
| chr5:149612292
|
C | T | 130 | a0001c0002t0005g0370a0001c0002t0006g0020a0001c0002t0006g0045others(127): Show | 133 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.458+2597C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612292 | ||||||
| chr5:149612316
|
G | C | 4 | a0004c0004t0004g0146a0005c0007t0003g0151a0005c0007t0003g0154others(1): Show | 4 | HG00597.hp1 HG02027.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+2621G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612316 | ||||||
| chr5:149612413
|
C | A | 1 | a0009c0013t0011g0011 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.458+2718C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612413 | ||||||
| chr5:149612424
|
C | T | 5 | a0001c0005t0004g0208a0001c0005t0004g0211a0001c0005t0004g0212others(2): Show | 5 | HG02055.hp1 HG02896.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+2729C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612424 | ||||||
| chr5:149612834
|
G | C | 1 | a0009c0013t0011g0011 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.458+3139G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612834 | ||||||
| chr5:149612873
|
A | C | 3 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039 | 3 | HG02280.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.458+3178A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612873 | ||||||
| chr5:149612880
|
C | T | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.458+3185C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612880 | ||||||
| chr5:149613041
|
G | A | 241 | a0001c0002t0005g0367a0001c0002t0005g0370a0001c0002t0006g0020others(238): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.458+3346G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613041 | ||||||
| chr5:149613097
|
G | A | 1 | a0006c0006t0007g0379 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.458+3402G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613097 | ||||||
| chr5:149613177
|
A | G | 8 | a0005c0011t0003g0324a0008c0009t0003g0319a0008c0009t0003g0320others(5): Show | 8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-3390A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613177 | ||||||
| chr5:149613187
|
T | C | 8 | a0005c0011t0003g0324a0008c0009t0003g0319a0008c0009t0003g0320others(5): Show | 8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-3380T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613187 | ||||||
| chr5:149613349
|
A | AT | 207 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(204): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.459-3203dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613349 | |||||
| chr5:149613403
|
G | A | 157 | a0001c0002t0005g0367a0001c0002t0006g0045a0001c0002t0006g0046others(154): Show | 166 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.459-3164G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613403 | ||||||
| chr5:149613404
|
T | C | 2 | a0011c0014t0023g0003a0011c0014t0035g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.459-3163T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613404 | ||||||
| chr5:149613507
|
C | T | 70 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(67): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.459-3060C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613507 | ||||||
| chr5:149613518
|
T | C | 2 | a0004c0004t0004g0143a0007c0008t0003g0238 | 2 | NA18997.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.459-3049T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613518 | ||||||
| chr5:149613663
|
C | T | 56 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(53): Show | 60 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.459-2904C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613663 | ||||||
| chr5:149613715
|
T | C | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2852T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613715 | ||||||
| chr5:149613764
|
C | CT | 5 | a0001c0002t0027g0337a0001c0005t0005g0201a0004c0004t0004g0220others(2): Show | 6 | HG02738.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2786dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613764 | |||||
| chr5:149613764
|
CT | C | 121 | a0001c0002t0006g0129a0001c0002t0015g0033a0002c0001t0001g0014others(118): Show | 121 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.459-2786delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613764 | |||||
| chr5:149613841
|
G | A | 1 | a0006c0006t0007g0358 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.459-2726G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613841 | ||||||
| chr5:149614012
|
C | T | 1 | a0001c0002t0015g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459-2555C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614012 | ||||||
| chr5:149614039
|
C | T | 119 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(116): Show | 119 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.459-2528C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614039 | ||||||
| chr5:149614068
|
G | GT | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2491dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149614068 | |||||
| chr5:149614123
|
A | AT | 126 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(123): Show | 126 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.459-2442dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149614123 | |||||
| chr5:149614327
|
A | G | 1 | a0009c0013t0011g0329 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.459-2240A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614327 | ||||||
| chr5:149614395
|
T | C | 2 | a0003c0003t0002g0012a0003c0012t0012g0099 | 3 | NA18951.hp1 NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.459-2172T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614395 | ||||||
| chr5:149614718
|
G | A | 1 | a0008c0009t0026g0318 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.459-1849G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614718 | ||||||
| chr5:149614812
|
G | A | 3 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0323 | 3 | HG00735.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.459-1755G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614812 | ||||||
| chr5:149614858
|
C | T | 1 | a0004c0004t0030g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-1709C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614858 | ||||||
| chr5:149614859
|
G | A | 1 | a0003c0003t0002g0284 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.459-1708G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614859 | ||||||
| chr5:149614866
|
A | G | 1 | a0001c0002t0020g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.459-1701A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614866 | ||||||
| chr5:149614951
|
C | T | 5 | a0002c0001t0001g0090a0002c0001t0001g0092a0002c0001t0001g0093others(2): Show | 5 | NA18940.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1616C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614951 | ||||||
| chr5:149615102
|
T | C | 80 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(77): Show | 80 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.459-1465T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615102 | ||||||
| chr5:149615244
|
T | G | 1 | a0001c0002t0008g0171 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.459-1323T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615244 | ||||||
| chr5:149615280
|
G | T | 1 | a0003c0003t0002g0274 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.459-1287G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615280 | ||||||
| chr5:149615305
|
A | AT | 102 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(99): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.459-1247dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149615305 | |||||
| chr5:149615305
|
AT | A | 6 | a0001c0002t0006g0118a0001c0002t0010g0166a0003c0003t0002g0313others(3): Show | 6 | HG01169.hp2 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-1247delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149615305 | |||||
| chr5:149615551
|
A | G | 2 | a0001c0002t0006g0127a0001c0002t0006g0129 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.459-1016A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615551 | ||||||
| chr5:149615616
|
G | A | 71 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(68): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.459-951G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615616 | ||||||
| chr5:149615658
|
G | A | 1 | a0006c0006t0007g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.459-909G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615658 | ||||||
| chr5:149615698
|
T | C | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.459-869T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615698 | ||||||
| chr5:149615792
|
T | C | 75 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(72): Show | 78 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.459-775T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615792 | ||||||
| chr5:149615829
|
T | C | 1 | a0005c0007t0003g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.459-738T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615829 | ||||||
| chr5:149615914
|
AC | A | 8 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-652delC | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615914 | ||||||
| chr5:149615946
|
C | G | 41 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(38): Show | 44 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.459-621C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615946 | ||||||
| chr5:149615972
|
C | T | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.459-595C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615972 | ||||||
| chr5:149616067
|
G | A | 4 | a0002c0001t0001g0136a0012c0016t0012g0053a0012c0016t0012g0072others(1): Show | 4 | HG02027.hp1 NA18612.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-500G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616067 | ||||||
| chr5:149616303
|
G | A | 1 | a0018c0020t0017g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.459-264G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616303 | ||||||
| chr5:149616316
|
C | T | 232 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(229): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.459-251C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616316 | ||||||
| chr5:149616388
|
C | T | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-179C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616388 | ||||||
| chr5:149616459
|
G | T | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.459-108G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616459 | ||||||
| chr5:149616539
|
C | T | 2 | a0001c0002t0006g0127a0001c0002t0006g0129 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.459-28C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616539 | ||||||
| chr5:149617052
|
C | T | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+286C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617052 | ||||||
| chr5:149617110
|
T | C | 1 | a0005c0007t0003g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.658+344T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617110 | ||||||
| chr5:149617295
|
T | C | 11 | a0001c0002t0006g0085a0001c0002t0006g0086a0001c0002t0006g0087others(8): Show | 11 | NA18939.hp1 NA18950.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.658+529T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617295 | ||||||
| chr5:149617628
|
G | A | 361 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(358): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.659-548G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617628 | ||||||
| chr5:149617687
|
C | T | 1 | a0004c0004t0009g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.659-489C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617687 | ||||||
| chr5:149617744
|
A | G | 14 | a0007c0008t0001g0026a0007c0008t0001g0051a0007c0008t0001g0052others(11): Show | 14 | HG00621.hp1 HG02074.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.659-432A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617744 | ||||||
| chr5:149617903
|
T | C | 2 | a0001c0002t0011g0365a0011c0014t0011g0275 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.659-273T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617903 | ||||||
| chr5:149618097
|
C | T | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-79C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618097 | ||||||
| chr5:149618123
|
A | G | 361 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(358): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.659-53A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618123 | ||||||
| chr5:149618132
|
A | T | 1 | a0004c0004t0004g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.659-44A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618132 | ||||||
| chr5:149618584
|
C | T | 9 | a0004c0004t0004g0013a0004c0004t0004g0243a0004c0004t0004g0244others(6): Show | 10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+278C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618584 | ||||||
| chr5:149618685
|
G | A | 88 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.790-253G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618685 | ||||||
| chr5:149618687
|
G | A | 88 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.790-251G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618687 | ||||||
| chr5:149618725
|
G | A | 1 | a0004c0004t0028g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.790-213G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618725 | ||||||
| chr5:149618814
|
T | G | 1 | a0002c0001t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.790-124T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618814 | ||||||
| chr5:149618816
|
C | T | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-122C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618816 | ||||||
| chr5:149618817
|
G | A | 52 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(49): Show | 56 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.790-121G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618817 | ||||||
| chr5:149619161
|
G | T | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.894+119G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619161 | ||||||
| chr5:149619229
|
G | C | 8 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+187G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619229 | ||||||
| chr5:149619284
|
G | A | 55 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(52): Show | 58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.894+242G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619284 | ||||||
| chr5:149619716
|
G | A | 9 | a0001c0002t0011g0365a0001c0002t0015g0032a0001c0002t0015g0033others(6): Show | 10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.895-638G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619716 | ||||||
| chr5:149619822
|
A | C | 259 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(256): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.895-532A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619822 | ||||||
| chr5:149619840
|
C | T | 1 | a0004c0004t0004g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.895-514C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619840 | ||||||
| chr5:149620014
|
A | C | 16 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.895-340A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620014 | ||||||
| chr5:149620072
|
C | CA | 7 | a0003c0003t0002g0007a0003c0003t0002g0278a0003c0012t0002g0276others(4): Show | 8 | HG03225.hp2 HG03579.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.895-267dupA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620072 | |||||
| chr5:149620072
|
CA | C | 137 | a0001c0002t0006g0084a0001c0002t0008g0168a0002c0001t0001g0014others(134): Show | 138 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.895-267delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620072 | |||||
| chr5:149620118
|
T | C | 1 | a0005c0011t0003g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.895-236T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620118 | ||||||
| chr5:149620171
|
A | G | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.895-183A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620171 | ||||||
| chr5:149620180
|
C | T | 1 | a0003c0003t0002g0248 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.895-174C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620180 | ||||||
| chr5:149620246
|
G | T | 4 | a0001c0005t0005g0185a0001c0005t0005g0192a0001c0005t0005g0193others(1): Show | 4 | HG00323.hp2 HG01943.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-108G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620246 | ||||||
| chr5:149620318
|
G | GC | 259 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(256): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.895-35dupC | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620318 | |||||
| chr5:149620476
|
C | T | 259 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(256): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1005+12C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620476 | ||||||
| chr5:149620567
|
C | T | 2 | a0003c0003t0002g0330a0003c0003t0002g0331 | 2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1005+103C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620567 | ||||||
| chr5:149620633
|
C | A | 1 | a0004c0010t0014g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1005+169C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620633 | ||||||
| chr5:149620688
|
G | A | 178 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(175): Show | 181 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1005+224G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620688 | ||||||
| chr5:149620692
|
A | G | 259 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(256): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1005+228A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620692 | ||||||
| chr5:149620714
|
C | T | 1 | a0005c0007t0003g0163 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1005+250C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620714 | ||||||
| chr5:149620780
|
G | A | 49 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(46): Show | 52 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1005+316G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620780 | ||||||
| chr5:149620829
|
C | CAAAAAAA others(3): Show |
13 | a0002c0001t0001g0047a0002c0001t0001g0056a0002c0001t0001g0066others(10): Show | 13 | HG00323.hp1 HG01256.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | |||||
| chr5:149620829
|
C | CAAAAAAA others(4): Show |
144 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(141): Show | 146 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(13): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | |||||
| chr5:149620829
|
C | CAAAAAAA others(5): Show |
21 | a0002c0001t0001g0092a0004c0004t0009g0009a0004c0004t0009g0257others(18): Show | 22 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | |||||
| chr5:149620837
|
G | A | 1 | a0004c0004t0004g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1005+373G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620837 | ||||||
| chr5:149620841
|
T | C | 88 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1005+377T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620841 | ||||||
| chr5:149620982
|
G | A | 1 | a0004c0004t0004g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1005+518G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620982 | ||||||
| chr5:149621378
|
C | T | 74 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(71): Show | 77 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1006-355C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621378 | ||||||
| chr5:149621379
|
G | A | 123 | a0002c0001t0001g0014a0002c0001t0001g0015a0002c0001t0001g0016others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1006-354G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621379 | ||||||
| chr5:149621432
|
T | A | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1006-301T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621432 | ||||||
| chr5:149621449
|
C | A | 16 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006-284C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621449 | ||||||
| chr5:149621455
|
A | G | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006-278A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621455 | ||||||
| chr5:149621540
|
C | T | 102 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(99): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1006-193C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621540 | ||||||
| chr5:149621720
|
T | C | 70 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(67): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1006-13T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621720 | ||||||
| chr5:149622128
|
C | CACACACA others(4): Show |
7 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0264others(4): Show | 8 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+67_1335+68ins others(11): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 149622128 | |||||
| chr5:149622334
|
A | G | 22 | a0001c0002t0006g0083a0001c0002t0006g0127a0001c0002t0006g0128others(19): Show | 25 | HG00544.hp1 HG00738.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.1335+272A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622334 | ||||||
| chr5:149622387
|
A | G | 102 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(99): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1335+325A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622387 | ||||||
| chr5:149622411
|
A | C | 1 | a0003c0003t0002g0307 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1335+349A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622411 | ||||||
| chr5:149622504
|
C | G | 234 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(231): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1335+442C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622504 | ||||||
| chr5:149622568
|
T | A | 1 | a0003c0003t0002g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1335+506T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622568 | ||||||
| chr5:149622666
|
C | T | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1335+604C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622666 | ||||||
| chr5:149622850
|
A | G | 2 | a0002c0001t0003g0272a0002c0001t0018g0271 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1335+788A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622850 | ||||||
| chr5:149622937
|
C | G | 18 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0274others(15): Show | 20 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1335+875C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622937 | ||||||
| chr5:149622969
|
A | T | 1 | a0003c0003t0002g0291 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1335+907A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622969 | ||||||
| chr5:149623008
|
C | G | 7 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(4): Show | 7 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+946C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623008 | ||||||
| chr5:149623198
|
A | G | 1 | a0001c0002t0006g0120 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1336-814A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623198 | ||||||
| chr5:149623232
|
C | T | 5 | a0001c0002t0006g0084a0001c0002t0006g0117a0001c0002t0006g0124others(2): Show | 5 | HG00408.hp2 HG02129.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-780C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623232 | ||||||
| chr5:149623615
|
C | T | 1 | a0001c0005t0005g0200 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1336-397C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623615 | ||||||
| chr5:149623718
|
A | C | 2 | a0016c0025t0013g0262a0016c0025t0013g0263 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1336-294A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623718 | ||||||
| chr5:149623934
|
A | G | 1 | a0001c0002t0006g0020 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1336-78A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623934 | ||||||
| chr5:149623966
|
T | C | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-46T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623966 | ||||||
| chr5:149624288
|
A | C | 256 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+148A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624288 | ||||||
| chr5:149624299
|
G | A | 1 | a0006c0006t0007g0357 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1464+159G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624299 | ||||||
| chr5:149624302
|
G | A | 18 | a0006c0006t0007g0333a0006c0006t0007g0351a0006c0006t0007g0354others(15): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464+162G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624302 | ||||||
| chr5:149624302
|
G | T | 16 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1464+162G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624302 | ||||||
| chr5:149624419
|
C | T | 16 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1464+279C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624419 | ||||||
| chr5:149624480
|
A | G | 7 | a0006c0006t0007g0333a0006c0006t0007g0357a0006c0006t0007g0361others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+340A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624480 | ||||||
| chr5:149624538
|
C | T | 1 | a0018c0020t0017g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1464+398C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624538 | ||||||
| chr5:149624539
|
C | T | 27 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0143others(24): Show | 28 | HG00438.hp1 HG00597.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1464+399C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624539 | ||||||
| chr5:149624553
|
C | T | 102 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(99): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1464+413C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624553 | ||||||
| chr5:149624582
|
T | C | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+442T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624582 | ||||||
| chr5:149624634
|
C | T | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1464+494C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624634 | ||||||
| chr5:149624649
|
C | CTGTAA | 255 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1464+510_1464+511i others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624649 | |||||
| chr5:149624688
|
T | G | 301 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(298): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1464+548T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624688 | ||||||
| chr5:149624819
|
G | A | 1 | a0014c0022t0004g0344 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1464+679G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624819 | ||||||
| chr5:149624900
|
G | GT | 51 | a0002c0001t0001g0017a0002c0001t0001g0067a0004c0004t0002g0228others(48): Show | 53 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1464+776dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | |||||
| chr5:149624900
|
G | GTT | 88 | a0001c0002t0004g0352a0001c0002t0006g0020a0001c0002t0006g0045others(85): Show | 93 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1464+775_1464+776d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | |||||
| chr5:149624900
|
G | GTTT | 111 | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(108): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1464+774_1464+776d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | |||||
| chr5:149624900
|
G | GTTTT | 10 | a0001c0002t0010g0169a0001c0002t0010g0170a0001c0005t0005g0191others(7): Show | 11 | HG00735.hp1 HG01099.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1464+773_1464+776d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | |||||
| chr5:149624938
|
G | A | 1 | a0001c0002t0008g0008 | 2 | NA18945.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1464+798G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624938 | ||||||
| chr5:149624938
|
G | T | 81 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(78): Show | 84 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1464+798G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624938 | ||||||
| chr5:149625015
|
C | G | 1 | a0005c0011t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1464+875C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625015 | ||||||
| chr5:149625135
|
T | A | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+995T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625135 | ||||||
| chr5:149625135
|
T | C | 284 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(281): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1464+995T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625135 | ||||||
| chr5:149625180
|
C | T | 53 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(50): Show | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1464+1040C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625180 | ||||||
| chr5:149625184
|
C | T | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1464+1044C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625184 | ||||||
| chr5:149625185
|
G | A | 70 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(67): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1464+1045G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625185 | ||||||
| chr5:149625264
|
A | C | 256 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+1124A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625264 | ||||||
| chr5:149625434
|
A | G | 256 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+1294A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625434 | ||||||
| chr5:149625526
|
G | T | 1 | a0004c0004t0004g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1464+1386G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625526 | ||||||
| chr5:149625611
|
T | A | 1 | a0001c0002t0010g0170 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1465-1465T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625611 | ||||||
| chr5:149625650
|
C | T | 2 | a0001c0002t0008g0254a0004c0004t0004g0180 | 2 | HG01243.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1465-1426C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625650 | ||||||
| chr5:149625675
|
G | A | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-1401G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625675 | ||||||
| chr5:149625682
|
G | A | 2 | a0002c0001t0001g0075a0002c0001t0001g0080 | 2 | HG02683.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1465-1394G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625682 | ||||||
| chr5:149625761
|
C | CCACA | 80 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(77): Show | 83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1465-1300_1465-129 others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149625761 | |||||
| chr5:149625849
|
G | A | 2 | a0001c0002t0011g0365a0011c0014t0011g0275 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1465-1227G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625849 | ||||||
| chr5:149625951
|
G | T | 3 | a0005c0011t0003g0324a0005c0011t0003g0336a0024c0037t0003g0363 | 3 | HG02622.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1465-1125G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625951 | ||||||
| chr5:149625997
|
A | G | 1 | a0002c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1465-1079A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625997 | ||||||
| chr5:149626211
|
C | T | 256 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1465-865C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626211 | ||||||
| chr5:149626241
|
A | AAC | 25 | a0001c0002t0005g0368a0001c0005t0004g0208a0001c0005t0004g0211others(22): Show | 28 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1465-790_1465-789d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
A | AACAC | 6 | a0001c0005t0005g0189a0002c0001t0001g0031a0002c0001t0001g0068others(3): Show | 6 | HG00609.hp2 HG04204.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-792_1465-789d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
A | AACACAC | 6 | a0002c0001t0001g0057a0002c0001t0001g0064a0002c0001t0001g0071others(3): Show | 6 | HG01978.hp2 HG02602.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-794_1465-789d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AAC | A | 45 | a0001c0002t0005g0367a0001c0002t0006g0020a0001c0002t0006g0045others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.1465-790_1465-789d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AACAC | A | 53 | a0001c0002t0005g0370a0001c0002t0005g0374a0001c0002t0006g0113others(50): Show | 55 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1465-792_1465-789d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AACACAC | A | 63 | a0001c0002t0006g0085a0001c0002t0006g0086a0001c0002t0006g0087others(60): Show | 63 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1465-794_1465-789d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AACACACA others(1): Show |
A | 13 | a0001c0002t0027g0337a0004c0004t0004g0013a0004c0004t0004g0239others(10): Show | 15 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1465-796_1465-789d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AACACACA others(3): Show |
A | 12 | a0006c0006t0007g0351a0006c0006t0007g0354a0006c0006t0007g0355others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1465-798_1465-789d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626241
|
AACACACA others(7): Show |
A | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-802_1465-789d others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | |||||
| chr5:149626244
|
A | C | 1 | a0001c0002t0010g0170 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1465-832A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626244 | ||||||
| chr5:149626282
|
ACACACG | A | 3 | a0003c0003t0002g0012a0003c0003t0002g0311a0008c0009t0002g0339 | 4 | HG03225.hp1 NA18951.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-792_1465-787d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626282 | |||||
| chr5:149626284
|
ACACG | A | 32 | a0003c0003t0002g0248a0003c0003t0002g0270a0003c0003t0002g0277others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1465-790_1465-787d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626284 | |||||
| chr5:149626286
|
ACG | A | 9 | a0003c0003t0002g0279a0003c0003t0002g0281a0003c0003t0002g0292others(6): Show | 9 | HG00438.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-788_1465-787d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626286 | |||||
| chr5:149626288
|
G | A | 25 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0274others(22): Show | 27 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1465-788G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626288 | ||||||
| chr5:149626288
|
G | T | 1 | a0007c0008t0001g0026 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1465-788G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626288 | ||||||
| chr5:149626473
|
C | G | 53 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(50): Show | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1465-603C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626473 | ||||||
| chr5:149626772
|
C | G | 203 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(200): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1465-304C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626772 | ||||||
| chr5:149626782
|
A | G | 8 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-294A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626782 | ||||||
| chr5:149626845
|
G | A | 55 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(52): Show | 58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1465-231G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626845 | ||||||
| chr5:149626863
|
A | G | 122 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(119): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1465-213A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626863 | ||||||
| chr5:149626883
|
A | G | 55 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(52): Show | 58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1465-193A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626883 | ||||||
| chr5:149626912
|
A | G | 1 | a0002c0001t0001g0071 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1465-164A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626912 | ||||||
| chr5:149626955
|
TCAGTGG | T | 104 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(101): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1465-117_1465-112d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626955 | |||||
| chr5:149627274
|
A | G | 243 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(240): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
splice_region_variant&intron_variant | LOW | c.1660+3A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627274 | ||||||
| chr5:149627275
|
C | T | 1 | a0002c0001t0001g0138 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.1660+4C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627275 | ||||||
| chr5:149627279
|
A | G | 55 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(52): Show | 58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1660+8A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627279 | ||||||
| chr5:149627316
|
A | G | 243 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(240): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1660+45A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627316 | ||||||
| chr5:149627323
|
A | G | 1 | a0008c0017t0013g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1660+52A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627323 | ||||||
| chr5:149627330
|
G | A | 1 | a0004c0004t0028g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1660+59G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627330 | ||||||
| chr5:149627333
|
G | A | 2 | a0004c0010t0022g0040a0004c0010t0022g0041 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1660+62G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627333 | ||||||
| chr5:149627342
|
C | T | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1660+71C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627342 | ||||||
| chr5:149627462
|
A | C | 9 | a0001c0002t0011g0365a0001c0002t0015g0032a0001c0002t0015g0033others(6): Show | 10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1660+191A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627462 | ||||||
| chr5:149627496
|
C | T | 157 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(154): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1660+225C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627496 | ||||||
| chr5:149627499
|
T | G | 7 | a0001c0002t0005g0367a0001c0005t0005g0001a0001c0005t0005g0002others(4): Show | 10 | HG00639.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1660+228T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627499 | ||||||
| chr5:149627619
|
A | G | 16 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0143others(13): Show | 17 | HG00597.hp2 HG02155.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.1660+348A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627619 | ||||||
| chr5:149627646
|
C | T | 84 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1660+375C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627646 | ||||||
| chr5:149627663
|
C | T | 53 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(50): Show | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1660+392C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627663 | ||||||
| chr5:149627778
|
G | A | 1 | a0001c0005t0005g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1660+507G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627778 | ||||||
| chr5:149628043
|
A | C | 3 | a0004c0010t0014g0325a0004c0010t0014g0326a0004c0010t0014g0328 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1661-766A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628043 | ||||||
| chr5:149628109
|
C | A | 139 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(136): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1661-700C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628109 | ||||||
| chr5:149628134
|
C | T | 1 | a0002c0001t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1661-675C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628134 | ||||||
| chr5:149628139
|
G | A | 1 | a0001c0002t0010g0170 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1661-670G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628139 | ||||||
| chr5:149628179
|
G | A | 53 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(50): Show | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1661-630G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628179 | ||||||
| chr5:149628186
|
G | A | 104 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(101): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1661-623G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628186 | ||||||
| chr5:149628223
|
C | T | 1 | a0004c0004t0030g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1661-586C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628223 | ||||||
| chr5:149628297
|
G | C | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-512G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628297 | ||||||
| chr5:149628311
|
G | A | 1 | a0002c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1661-498G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628311 | ||||||
| chr5:149628403
|
C | G | 157 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(154): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1661-406C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628403 | ||||||
| chr5:149628439
|
A | G | 243 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(240): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1661-370A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628439 | ||||||
| chr5:149628459
|
G | A | 73 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(70): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1661-350G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628459 | ||||||
| chr5:149628485
|
A | G | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-324A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628485 | ||||||
| chr5:149628510
|
G | A | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-299G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628510 | ||||||
| chr5:149628587
|
C | T | 7 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661-222C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628587 | ||||||
| chr5:149628751
|
T | A | 4 | a0008c0017t0013g0251a0008c0017t0013g0252a0016c0025t0013g0262others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1661-58T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628751 | ||||||
| chr5:149628777
|
C | T | 1 | a0001c0005t0005g0200 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1661-32C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628777 | ||||||
| chr5:149628998
|
C | T | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1818+32C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149628998 | ||||||
| chr5:149629004
|
G | A | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1818+38G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629004 | ||||||
| chr5:149629188
|
C | G | 104 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(101): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1818+222C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629188 | ||||||
| chr5:149629215
|
G | GATTC | 17 | a0002c0001t0003g0272a0002c0001t0018g0271a0005c0011t0001g0037others(14): Show | 17 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1818+279_1818+282d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | |||||
| chr5:149629215
|
G | GATTCATT others(1): Show |
5 | a0005c0011t0001g0038a0005c0011t0003g0324a0005c0011t0003g0336others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+275_1818+282d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | |||||
| chr5:149629215
|
G | GATTCATT others(5): Show |
3 | a0005c0011t0001g0039a0005c0011t0003g0372a0006c0006t0034g0269 | 3 | HG02559.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1818+271_1818+282d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | |||||
| chr5:149629215
|
GATTC | G | 156 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(153): Show | 165 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1818+279_1818+282d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | |||||
| chr5:149629215
|
GATTCATT others(1): Show |
G | 115 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(112): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1818+275_1818+282d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | |||||
| chr5:149629281
|
A | G | 8 | a0004c0004t0004g0013a0004c0004t0004g0243a0004c0004t0004g0244others(5): Show | 9 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1818+315A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629281 | ||||||
| chr5:149629352
|
T | A | 33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1818+386T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629352 | ||||||
| chr5:149629380
|
T | G | 1 | a0005c0007t0003g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1818+414T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629380 | ||||||
| chr5:149629419
|
T | G | 1 | a0005c0011t0003g0324 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1818+453T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629419 | ||||||
| chr5:149629458
|
G | A | 276 | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(273): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1818+492G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629458 | ||||||
| chr5:149629553
|
C | A | 1 | a0005c0011t0001g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1818+587C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629553 | ||||||
| chr5:149629573
|
G | A | 1 | a0009c0013t0021g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1818+607G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629573 | ||||||
| chr5:149629581
|
T | A | 1 | a0001c0002t0010g0170 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1818+615T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629581 | ||||||
| chr5:149629590
|
G | A | 1 | a0004c0004t0028g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1818+624G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629590 | ||||||
| chr5:149629755
|
G | A | 7 | a0006c0006t0007g0333a0006c0006t0007g0357a0006c0006t0007g0361others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+789G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629755 | ||||||
| chr5:149629769
|
C | T | 1 | a0004c0004t0004g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1818+803C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629769 | ||||||
| chr5:149629796
|
G | A | 51 | a0001c0002t0006g0020a0001c0002t0006g0045a0001c0002t0006g0046others(48): Show | 54 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1818+830G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629796 | ||||||
| chr5:149629877
|
C | T | 39 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(36): Show | 41 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1818+911C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629877 | ||||||
| chr5:149629933
|
T | A | 7 | a0008c0009t0003g0319a0008c0009t0003g0320a0008c0009t0003g0321others(4): Show | 7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+967T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629933 | ||||||
| chr5:149629947
|
C | T | 14 | a0004c0004t0009g0009a0004c0004t0009g0257a0004c0004t0009g0258others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1818+981C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629947 | ||||||
| chr5:149629958
|
T | C | 8 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1818+992T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629958 | ||||||
| chr5:149629970
|
A | G | 3 | a0004c0004t0004g0221a0004c0004t0004g0232a0004c0004t0004g0233 | 3 | NA18949.hp1 NA18986.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1818+1004A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629970 | ||||||
| chr5:149630010
|
G | A | 2 | a0018c0020t0017g0176a0018c0020t0017g0177 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1818+1044G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630010 | ||||||
| chr5:149630130
|
C | A | 1 | a0020c0032t0009g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1818+1164C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630130 | ||||||
| chr5:149630188
|
G | A | 41 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(38): Show | 43 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1818+1222G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630188 | ||||||
| chr5:149630252
|
T | G | 1 | a0004c0004t0004g0232 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1818+1286T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630252 | ||||||
| chr5:149630334
|
C | T | 3 | a0002c0001t0001g0054a0002c0001t0001g0079a0002c0001t0001g0081 | 3 | HG02735.hp2 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1818+1368C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630334 | ||||||
| chr5:149630529
|
C | A | 1 | a0004c0004t0009g0009 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1819-1453C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630529 | ||||||
| chr5:149630615
|
C | G | 41 | a0004c0004t0002g0228a0004c0004t0004g0006a0004c0004t0004g0013others(38): Show | 43 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1819-1367C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630615 | ||||||
| chr5:149630650
|
C | T | 2 | a0016c0025t0013g0262a0016c0025t0013g0263 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1819-1332C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630650 | ||||||
| chr5:149631070
|
C | T | 2 | a0001c0002t0015g0033a0001c0002t0015g0034 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1819-912C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631070 | ||||||
| chr5:149631116
|
T | TTTTC | 5 | a0005c0011t0001g0037a0005c0011t0001g0038a0005c0011t0001g0039others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-847_1819-844d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631116 | |||||
| chr5:149631132
|
CTTTCTTC others(9): Show |
C | 4 | a0003c0012t0002g0164a0012c0016t0012g0053a0012c0016t0012g0072others(1): Show | 4 | HG02027.hp1 HG02523.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-847_1819-832d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631132 | |||||
| chr5:149631135
|
TCTTCCTT others(9): Show |
T | 2 | a0003c0003t0002g0301a0003c0003t0002g0302 | 2 | NA18948.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1819-834_1819-819d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631135 | |||||
| chr5:149631136
|
CTTCCTTC others(5): Show |
C | 70 | a0003c0003t0002g0007a0003c0003t0002g0010a0003c0003t0002g0012others(67): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1819-834_1819-823d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631136 | |||||
| chr5:149631139
|
C | T | 3 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1819-843C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631139 | ||||||
| chr5:149631140
|
CTTCCTTC others(1): Show |
C | 3 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1819-834_1819-827d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631140 | |||||
| chr5:149631151
|
C | T | 1 | a0005c0035t0003g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1819-831C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631151 | ||||||
| chr5:149631167
|
CCTTT | C | 49 | a0002c0001t0001g0049a0004c0004t0002g0228a0004c0004t0004g0006others(46): Show | 51 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1819-810_1819-807d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631167 | |||||
| chr5:149631172
|
CTTTT | C | 4 | a0003c0003t0002g0303a0003c0003t0002g0307a0003c0003t0008g0296others(1): Show | 4 | NA18960.hp2 NA18961.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-806_1819-803d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631172 | |||||
| chr5:149631180
|
CT | C | 42 | a0001c0005t0005g0192a0004c0004t0002g0228a0004c0004t0004g0006others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1819-789delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631180 | |||||
| chr5:149631195
|
G | A | 1 | a0003c0012t0002g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1819-787G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631195 | ||||||
| chr5:149631235
|
G | A | 4 | a0009c0013t0011g0011a0009c0013t0011g0329a0009c0013t0021g0108others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-747G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631235 | ||||||
| chr5:149631240
|
C | T | 78 | a0001c0002t0015g0032a0001c0002t0015g0033a0001c0002t0015g0034others(75): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1819-742C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631240 | ||||||
| chr5:149631568
|
C | T | 1 | a0003c0003t0002g0278 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1819-414C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631568 | ||||||
| chr5:149631681
|
T | TCCTTGAC others(3): Show |
33 | a0005c0007t0003g0144a0005c0007t0003g0145a0005c0007t0003g0147others(30): Show | 33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1819-300_1819-291d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631681 | |||||
| chr5:149631748
|
G | A | 1 | a0001c0002t0005g0368 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1819-234G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631748 | ||||||
| chr5:149631789
|
C | A | 2 | a0008c0017t0013g0251a0008c0017t0013g0252 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1819-193C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631789 | ||||||
| chr5:149631861
|
C | T | 1 | a0002c0001t0001g0024 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1819-121C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631861 |