Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9181 |
|---|---|
| ensemblid | ENSG00000116584.22 |
| hgncid | 682 |
| symbol | ARHGEF2 |
| name | Rho/Rac guanine nucleotide exchange factor 2 |
| refseq_nuc | NM_001162383.2 |
| refseq_prot | NP_001155855.1 |
| ensembl_nuc | ENST00000361247.9 |
| ensembl_prot | ENSP00000354837.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 155946854 |
| end | 155978547 |
| strand | - |
| ver | v1.2 |
| region | chr1:155946854-155978547 |
| region5000 | chr1:155941854-155983547 |
| regionname0 | ARHGEF2_chr1_155946854_155978547 |
| regionname5000 | ARHGEF2_chr1_155941854_155983547 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 986 | 275 | 82 | 50 | 95 | 12 | 34 | 65 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0002 | 0/0 | 986 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0003 | 0/0 | 986 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0004 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2961 | 269 | 78 | 49 | 94 | 12 | 34 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0002 | 0/0 | 2961 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0003 | 0/0 | 2961 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0004 | 0/0 | 2961 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0005 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0006 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| c0007 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1209 | 272 | 87 | 48 | 96 | 9 | 30 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0002 | 0/0 | 1209 | 7 | 1 | 2 | 0 | 2 | 2 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0003 | 0/0 | 1209 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0004 | 0/0 | 1209 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0005 | 0/0 | 1209 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0006 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| t0007 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| 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 | 14 | 0 | 9 | 4 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0002 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0009 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2961 | 269 | 78 | 49 | 94 | 12 | 34 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0003 | 0/0 | 2961 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0006 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0007 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0002c0002 | 0/0 | 2961 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0003c0004 | 0/0 | 2961 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0004c0005 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4169 | 257 | 77 | 47 | 92 | 9 | 30 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0002 | 0/0 | 4169 | 7 | 1 | 2 | 0 | 2 | 2 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0003 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0004 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0005 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0006 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0001t0007 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0003t0001 | 0/0 | 4169 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0006t0001 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0001c0007t0001 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0002c0002t0001 | 0/0 | 4169 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0003c0004t0001 | 0/0 | 4169 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| a0004c0005t0001 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | copy fasta | chr1 | 155941854 | 155983547 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 9 | 4 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0002 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0009 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0004c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0075 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02809 | hp2 | a0004 | c0005 | t0001 | g0157 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0212 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18963 | hp1 | a0001 | c0006 | t0001 | g0100 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18985 | hp2 | a0003 | c0004 | t0001 | g0067 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19067 | hp1 | a0003 | c0004 | t0001 | g0073 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19077 | hp2 | a0003 | c0004 | t0001 | g0069 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0142 | SAS | GIH | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0113 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155947968
|
C | A | 1 | a0003 | 3 | NA18985.hp2 NA19067.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.2935G>T | p.Gly979Trp | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 3055/4169 | 2935/2961 | 979/986 | chr1 | 155947968 | ||
| chr1:155950335
|
C | A | 1 | a0002 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.2851G>T | p.Gly951Cys | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/22 | 2971/4169 | 2851/2961 | 951/986 | chr1 | 155950335 | ||
| chr1:155957716
|
C | T | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1712G>A | p.Arg571His | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/22 | 1832/4169 | 1712/2961 | 571/986 | chr1 | 155957716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155950455
|
G | A | 1 | a0001c0006 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.2731C>T | p.Leu911Leu | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/22 | 2851/4169 | 2731/2961 | 911/986 | chr1 | 155950455 | ||
| chr1:155951747
|
C | A | 1 | a0001c0003 | 4 | HG01109.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.2202G>T | p.Pro734Pro | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 18/22 | 2322/4169 | 2202/2961 | 734/986 | chr1 | 155951747 | ||
| chr1:155961839
|
G | A | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1290C>T | p.Asp430Asp | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/22 | 1410/4169 | 1290/2961 | 430/986 | chr1 | 155961839 | ||
| chr1:155965367
|
T | C | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.516A>G | p.Ser172Ser | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/22 | 636/4169 | 516/2961 | 172/986 | chr1 | 155965367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155947129
|
G | T | 1 | a0001c0001t0003 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 813 | chr1 | 155947129 | |||||
| chr1:155947531
|
G | A | 1 | a0001c0001t0004 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 411 | chr1 | 155947531 | |||||
| chr1:155947598
|
G | C | 2 | a0001c0001t0002a0001c0001t0005 | 8 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 344 | chr1 | 155947598 | |||||
| chr1:155947801
|
T | A | 1 | a0001c0001t0005 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 141 | chr1 | 155947801 | |||||
| chr1:155947920
|
G | A | 1 | a0001c0001t0006 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 22 | chr1 | 155947920 | |||||
| chr1:155947927
|
G | C | 1 | a0001c0001t0007 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 15 | chr1 | 155947927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155948089
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2888-74A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948089 | ||||||
| chr1:155948222
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2888-207G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948222 | ||||||
| chr1:155948365
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2888-350G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948365 | ||||||
| chr1:155948465
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2888-450T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948465 | ||||||
| chr1:155948563
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2888-548C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948563 | ||||||
| chr1:155948666
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2888-651A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948666 | ||||||
| chr1:155948793
|
G | C | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2888-778C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948793 | ||||||
| chr1:155948828
|
G | A | 12 | a0001c0001t0001g0181a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2888-813C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948828 | ||||||
| chr1:155948908
|
C | T | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2888-893G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948908 | ||||||
| chr1:155949264
|
T | TAAATA | 8 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 10 | HG01243.hp1 HG01515.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.2887+1030_2887+103 others(9): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949264 | ||||||
| chr1:155949264
|
T | TAAATAAA others(3): Show |
1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2887+1025_2887+103 others(14): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949264 | ||||||
| chr1:155949443
|
G | A | 1 | a0001c0003t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2887+856C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949443 | ||||||
| chr1:155949557
|
C | T | 2 | a0001c0003t0001g0027a0001c0003t0001g0201 | 3 | HG01109.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2887+742G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949557 | ||||||
| chr1:155949742
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2887+557G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949742 | ||||||
| chr1:155949743
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2887+556C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949743 | ||||||
| chr1:155949862
|
G | A | 1 | a0001c0003t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2887+437C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949862 | ||||||
| chr1:155949998
|
G | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0077others(1): Show | 5 | HG00544.hp1 HG02132.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2887+301C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949998 | ||||||
| chr1:155950048
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2887+251G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155950048 | ||||||
| chr1:155950489
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0124 | 3 | HG01069.hp2 HG01071.hp2 HG01496.hp1 |
splice_region_variant&intron_variant | LOW | c.2704-7T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 20/21 | chr1 | 155950489 | ||||||
| chr1:155950574
|
C | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2704-92G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 20/21 | chr1 | 155950574 | ||||||
| chr1:155952377
|
G | A | 3 | a0001c0003t0001g0027a0001c0003t0001g0201a0001c0003t0001g0212 | 4 | HG01109.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1985-142C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 15/21 | chr1 | 155952377 | ||||||
| chr1:155952404
|
C | T | 11 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0081others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1985-169G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 15/21 | chr1 | 155952404 | ||||||
| chr1:155953179
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1784-351G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953179 | ||||||
| chr1:155953265
|
C | CA | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1784-438dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953265 | ||||||
| chr1:155953265
|
C | CAA | 6 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 6 | HG00609.hp2 HG03195.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-439_1784-438d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953265 | ||||||
| chr1:155953692
|
A | C | 5 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-864T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953692 | ||||||
| chr1:155953716
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1784-888G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953716 | ||||||
| chr1:155953746
|
C | CA | 10 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0080others(7): Show | 12 | HG01192.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784-919dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953746 | ||||||
| chr1:155953746
|
CA | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0001g0068others(3): Show | 6 | HG02135.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-919delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953746 | ||||||
| chr1:155953763
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0149 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1784-935T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953763 | ||||||
| chr1:155953980
|
G | T | 23 | a0001c0001t0001g0181a0001c0001t0001g0190a0001c0001t0001g0191others(20): Show | 25 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1783+922C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953980 | ||||||
| chr1:155954016
|
C | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1783+886G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954016 | ||||||
| chr1:155954085
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1783+817G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954085 | ||||||
| chr1:155954127
|
A | AT | 5 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0031others(2): Show | 9 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1783+774dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954127 | ||||||
| chr1:155954127
|
A | ATT | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1783+773_1783+774d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954127 | ||||||
| chr1:155954282
|
C | CT | 26 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0051others(23): Show | 26 | HG01496.hp2 HG01934.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1783+619dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954282 | ||||||
| chr1:155954282
|
C | CTT | 63 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(60): Show | 80 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1783+618_1783+619d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954282 | ||||||
| chr1:155954285
|
T | C | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1783+617A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954285 | ||||||
| chr1:155954323
|
G | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1783+579C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954323 | ||||||
| chr1:155954328
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1783+574C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954328 | ||||||
| chr1:155954446
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+456T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954446 | ||||||
| chr1:155954478
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+424G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954478 | ||||||
| chr1:155954489
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+413G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954489 | ||||||
| chr1:155954519
|
A | G | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1783+383T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954519 | ||||||
| chr1:155954521
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+381G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954521 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0001t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0001t0002g0103 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0134 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0053 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0036 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(314): Show |
15 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0063others(12): Show | 15 | HG01168.hp1 HG01192.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783+312_1783+313i others(323): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954589
|
A | ATCTACTT others(315): Show |
1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(324): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | ||||||
| chr1:155954613
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02071.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1783+289T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954613 | ||||||
| chr1:155954631
|
A | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+271T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954631 | ||||||
| chr1:155954714
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1783+188T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954714 | ||||||
| chr1:155954755
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1783+147A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954755 | ||||||
| chr1:155954852
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1783+50A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954852 | ||||||
| chr1:155955039
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1716-70A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955039 | ||||||
| chr1:155955074
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1716-105T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955074 | ||||||
| chr1:155955150
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1716-181G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955150 | ||||||
| chr1:155955188
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0148a0001c0001t0001g0153others(1): Show | 4 | NA18985.hp1 NA19012.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716-219G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955188 | ||||||
| chr1:155955465
|
T | C | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716-496A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955465 | ||||||
| chr1:155955693
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1716-724G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955693 | ||||||
| chr1:155955779
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1716-810C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955779 | ||||||
| chr1:155955908
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1716-939C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955908 | ||||||
| chr1:155956260
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0044others(8): Show | 14 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1716-1291C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956260 | ||||||
| chr1:155956366
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0147 | 3 | HG02129.hp2 HG02132.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1715+1347G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956366 | ||||||
| chr1:155956426
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1715+1287G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956426 | ||||||
| chr1:155956609
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1715+1104T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956609 | ||||||
| chr1:155956887
|
C | CA | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1715+825dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956887 | ||||||
| chr1:155956887
|
C | CAA | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0016others(33): Show | 42 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1715+824_1715+825d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956887 | ||||||
| chr1:155957038
|
TA | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0123a0001c0001t0001g0209others(1): Show | 6 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1715+674delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957038 | ||||||
| chr1:155957402
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1715+311G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957402 | ||||||
| chr1:155957421
|
T | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0183others(5): Show | 9 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1715+292A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957421 | ||||||
| chr1:155957459
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0230 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1715+254G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957459 | ||||||
| chr1:155957899
|
A | G | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-17T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957899 | ||||||
| chr1:155957950
|
T | A | 1 | a0001c0003t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1546-68A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957950 | ||||||
| chr1:155957961
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1546-79C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957961 | ||||||
| chr1:155958053
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1546-171G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958053 | ||||||
| chr1:155958096
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1546-214G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958096 | ||||||
| chr1:155958170
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1545+150G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958170 | ||||||
| chr1:155958172
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1545+148C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958172 | ||||||
| chr1:155958194
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0038others(11): Show | 18 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1545+126C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958194 | ||||||
| chr1:155958243
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0138 | 2 | NA18992.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1545+77G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958243 | ||||||
| chr1:155958282
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1545+38A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958282 | ||||||
| chr1:155958441
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1469-45A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958441 | ||||||
| chr1:155958451
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1469-55G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958451 | ||||||
| chr1:155958574
|
A | AT | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(78): Show | 99 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1469-179dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958574 | ||||||
| chr1:155958679
|
G | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1469-283C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958679 | ||||||
| chr1:155959041
|
T | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0209a0001c0001t0001g0210 | 5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469-645A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959041 | ||||||
| chr1:155959664
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1469-1268G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959664 | ||||||
| chr1:155959701
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1469-1305A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959701 | ||||||
| chr1:155959705
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1469-1309A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959705 | ||||||
| chr1:155959771
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1469-1375G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959771 | ||||||
| chr1:155959853
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1469-1457G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959853 | ||||||
| chr1:155959882
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1469-1486G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959882 | ||||||
| chr1:155959910
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1469-1514C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959910 | ||||||
| chr1:155960068
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1468+1593A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960068 | ||||||
| chr1:155960468
|
TA | T | 12 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp2 HG02132.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468+1192delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960468 | ||||||
| chr1:155960482
|
A | AG | 75 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(72): Show | 92 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1468+1178_1468+117 others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960482 | ||||||
| chr1:155960482
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0116others(2): Show | 5 | HG01515.hp2 HG01981.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+1179T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960482 | ||||||
| chr1:155960766
|
C | T | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+895G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960766 | ||||||
| chr1:155960987
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1468+674G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960987 | ||||||
| chr1:155961059
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1468+602G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961059 | ||||||
| chr1:155961162
|
T | C | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+499A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961162 | ||||||
| chr1:155961194
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0030others(3): Show | 10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+467C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961194 | ||||||
| chr1:155961274
|
C | CT | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0138others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+386dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961274 | ||||||
| chr1:155961475
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1468+186A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961475 | ||||||
| chr1:155961577
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(71): Show | 91 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1468+84C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961577 | ||||||
| chr1:155961999
|
G | T | 1 | a0001c0003t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1220-90C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 10/21 | chr1 | 155961999 | ||||||
| chr1:155963211
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0183others(4): Show | 8 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-28A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963211 | ||||||
| chr1:155963261
|
A | G | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.725-78T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963261 | ||||||
| chr1:155963344
|
CT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.725-162delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963344 | ||||||
| chr1:155963506
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.725-323G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963506 | ||||||
| chr1:155963595
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.725-412G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963595 | ||||||
| chr1:155963675
|
AT | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.725-493delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963675 | ||||||
| chr1:155963679
|
T | A | 1 | a0001c0001t0002g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.725-496A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963679 | ||||||
| chr1:155964018
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0120 | 2 | HG00099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.725-835C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964018 | ||||||
| chr1:155964032
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.725-849G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964032 | ||||||
| chr1:155964144
|
CAA | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(58): Show | 77 | HG00280.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.724+842_724+843del others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964144 | ||||||
| chr1:155964154
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+834T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964154 | ||||||
| chr1:155964155
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.724+833T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964155 | ||||||
| chr1:155964156
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+832T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964156 | ||||||
| chr1:155964157
|
A | AATATATA others(27): Show |
1 | a0001c0001t0001g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.724+830_724+831ins others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | ||||||
| chr1:155964157
|
A | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0084others(2): Show | 5 | HG00735.hp1 HG01516.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+831T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | ||||||
| chr1:155964157
|
AAAAAAAA others(27): Show |
A | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0006g0106 | 3 | NA18993.hp2 NA19054.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.724+797_724+830del others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | ||||||
| chr1:155964158
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+830T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964158 | ||||||
| chr1:155964159
|
A | AT | 9 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0038others(6): Show | 13 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+828_724+829ins others(1): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | ||||||
| chr1:155964159
|
A | ATATAT | 2 | a0001c0001t0001g0012a0001c0001t0001g0066 | 3 | HG01070.hp2 HG01071.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.724+828_724+829ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | ||||||
| chr1:155964159
|
A | T | 25 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(22): Show | 25 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.724+829T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | ||||||
| chr1:155964159
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0005a0001c0001t0001g0058 | 4 | HG00621.hp2 HG02083.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+811_724+828del others(18): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | ||||||
| chr1:155964160
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+828T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964160 | ||||||
| chr1:155964160
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+815_724+827del others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964160 | ||||||
| chr1:155964161
|
A | ATATAT | 3 | a0001c0001t0001g0072a0001c0001t0002g0103a0003c0004t0001g0073 | 3 | HG01168.hp1 HG01168.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.724+826_724+827ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | ||||||
| chr1:155964161
|
A | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 164 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.724+827T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | ||||||
| chr1:155964161
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.724+815_724+826del others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | ||||||
| chr1:155964162
|
AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0001g0048a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+815_724+825del others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964162 | ||||||
| chr1:155964163
|
A | ATATAT | 3 | a0001c0001t0001g0097a0001c0003t0001g0027a0001c0003t0001g0201 | 4 | HG01109.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+824_724+825ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | ||||||
| chr1:155964163
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.724+825T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | ||||||
| chr1:155964163
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.724+825T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | ||||||
| chr1:155964164
|
AAAAATAT others(4): Show |
A | 6 | a0001c0001t0001g0181a0001c0001t0001g0190a0001c0001t0001g0196others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+813_724+823del others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964164 | ||||||
| chr1:155964164
|
AAAAATAT others(6): Show |
A | 1 | a0001c0001t0001g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.724+811_724+823del others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964164 | ||||||
| chr1:155964165
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.724+823T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | ||||||
| chr1:155964165
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.724+803_724+822del others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | ||||||
| chr1:155964165
|
AAAATATA others(15): Show |
A | 1 | a0001c0001t0001g0023 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.724+801_724+822del others(22): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | ||||||
| chr1:155964167
|
A | AAAAATAT others(36): Show |
1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.724+820_724+821ins others(43): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.724+820_724+821ins others(18): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.724+820_724+821ins others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AAAATATA others(35): Show |
2 | a0002c0002t0001g0228a0002c0002t0001g0229 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.724+820_724+821ins others(42): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AAAATATA others(39): Show |
1 | a0001c0001t0001g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.724+820_724+821ins others(46): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AAATATAT others(38): Show |
2 | a0002c0002t0001g0028a0002c0002t0001g0222 | 3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.724+820_724+821ins others(45): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AATAT | 6 | a0001c0001t0001g0024a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+817_724+820dup others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | AATATATA others(39): Show |
1 | a0001c0001t0001g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.724+820_724+821ins others(46): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964167
|
A | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.724+821T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | ||||||
| chr1:155964168
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.724+819_724+820ins others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964168 | ||||||
| chr1:155964168
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.724+809_724+819del others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964168 | ||||||
| chr1:155964169
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0209others(1): Show | 7 | HG01891.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+819A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964169 | ||||||
| chr1:155964170
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724+818T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964170 | ||||||
| chr1:155964171
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0210 | 4 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+817A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964171 | ||||||
| chr1:155964172
|
A | ATATATG | 18 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 22 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.724+815_724+816ins others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964172 | ||||||
| chr1:155964174
|
A | ATATATG | 4 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0056others(1): Show | 5 | HG02630.hp2 HG03834.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+813_724+814ins others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | ||||||
| chr1:155964174
|
A | ATATG | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(30): Show | 46 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.724+813_724+814ins others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | ||||||
| chr1:155964174
|
A | ATATGTAT others(27): Show |
1 | a0001c0001t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.724+813_724+814ins others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | ||||||
| chr1:155964174
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+814T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | ||||||
| chr1:155964175
|
T | C | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+813A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964175 | ||||||
| chr1:155964176
|
A | ATG | 19 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 20 | HG00099.hp1 HG00099.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.724+811_724+812ins others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964176 | ||||||
| chr1:155964176
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0038others(11): Show | 18 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.724+812T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964176 | ||||||
| chr1:155964178
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.724+810T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964178 | ||||||
| chr1:155964180
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(64): Show | 83 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.724+808T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964180 | ||||||
| chr1:155964189
|
T | C | 2 | a0001c0003t0001g0027a0001c0003t0001g0201 | 3 | HG01109.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.724+799A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964189 | ||||||
| chr1:155964193
|
TATATAC | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0185 | 3 | HG00140.hp2 HG01978.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.724+789_724+794del others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964193 | ||||||
| chr1:155964195
|
T | C | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+793A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964195 | ||||||
| chr1:155964196
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.724+792T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964196 | ||||||
| chr1:155964197
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.724+791A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964197 | ||||||
| chr1:155964199
|
C | CAT | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0120 | 3 | HG00099.hp2 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.724+787_724+788dup others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | ||||||
| chr1:155964199
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0131others(5): Show | 10 | HG00621.hp2 HG01975.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+789G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | ||||||
| chr1:155964199
|
CAT | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(1): Show | 4 | HG01258.hp1 HG02451.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+787_724+788del others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | ||||||
| chr1:155964201
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0185others(1): Show | 5 | HG00140.hp2 HG01433.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+787A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964201 | ||||||
| chr1:155964202
|
A | G | 1 | a0001c0001t0001g0005 | 3 | HG00621.hp2 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.724+786T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964202 | ||||||
| chr1:155964215
|
TA | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0040others(6): Show | 13 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+772delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964215 | ||||||
| chr1:155964216
|
A | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 7 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.724+772T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964216 | ||||||
| chr1:155964227
|
A | T | 1 | a0001c0001t0001g0005 | 3 | HG00621.hp2 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.724+761T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964227 | ||||||
| chr1:155964641
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+347G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964641 | ||||||
| chr1:155964748
|
C | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+240G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964748 | ||||||
| chr1:155964892
|
CA | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.724+95delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964892 | ||||||
| chr1:155964908
|
A | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0209a0001c0001t0001g0210 | 5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+80T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964908 | ||||||
| chr1:155965141
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.581-10T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/21 | chr1 | 155965141 | ||||||
| chr1:155965141
|
A | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.581-10T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/21 | chr1 | 155965141 | ||||||
| chr1:155965450
|
G | A | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.471-38C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965450 | ||||||
| chr1:155965453
|
C | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.471-41G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965453 | ||||||
| chr1:155965501
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471-89C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965501 | ||||||
| chr1:155965893
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.341-133A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155965893 | ||||||
| chr1:155966009
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.341-249T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966009 | ||||||
| chr1:155966058
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.341-298A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966058 | ||||||
| chr1:155966236
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340+180G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966236 | ||||||
| chr1:155966359
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.340+57A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966359 | ||||||
| chr1:155966910
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-23C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155966910 | ||||||
| chr1:155967002
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.209-115G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967002 | ||||||
| chr1:155967301
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-414C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967301 | ||||||
| chr1:155967371
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0034others(14): Show | 21 | HG00438.hp1 HG00621.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.209-484T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967371 | ||||||
| chr1:155967599
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-712G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967599 | ||||||
| chr1:155967734
|
A | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.209-847T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967734 | ||||||
| chr1:155967833
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.209-946G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967833 | ||||||
| chr1:155968111
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.208+1045T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968111 | ||||||
| chr1:155968153
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.208+1003T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968153 | ||||||
| chr1:155968202
|
CT | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.208+953delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968202 | ||||||
| chr1:155968284
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+872G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968284 | ||||||
| chr1:155968361
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.208+795A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968361 | ||||||
| chr1:155968740
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.208+416T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968740 | ||||||
| chr1:155969084
|
G | GA | 4 | a0002c0002t0001g0028a0002c0002t0001g0222a0002c0002t0001g0228others(1): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+71dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155969084 | ||||||
| chr1:155969445
|
G | A | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-145C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969445 | ||||||
| chr1:155969458
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-158T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969458 | ||||||
| chr1:155969585
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-285T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969585 | ||||||
| chr1:155969825
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-525G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969825 | ||||||
| chr1:155969886
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0112 | 3 | HG00280.hp2 HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.64-586C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969886 | ||||||
| chr1:155970064
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.64-764C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970064 | ||||||
| chr1:155970373
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-1073G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970373 | ||||||
| chr1:155970472
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-1172G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970472 | ||||||
| chr1:155970486
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-1186C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970486 | ||||||
| chr1:155970942
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-1642G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970942 | ||||||
| chr1:155970972
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-1672T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970972 | ||||||
| chr1:155971157
|
T | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 123 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.64-1857A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971157 | ||||||
| chr1:155971300
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-2000C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971300 | ||||||
| chr1:155971387
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.64-2087C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971387 | ||||||
| chr1:155971579
|
C | CA | 9 | a0001c0001t0001g0090a0001c0001t0001g0200a0001c0001t0001g0227others(6): Show | 10 | HG00280.hp1 HG01192.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2280dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | ||||||
| chr1:155971579
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0038a0001c0001t0001g0108a0001c0001t0001g0121others(3): Show | 6 | HG00280.hp2 HG01496.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2290_64-2280dup others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | ||||||
| chr1:155971579
|
C | CAAAAAAA others(5): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(80): Show | 105 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.64-2291_64-2280dup others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | ||||||
| chr1:155971579
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0119a0001c0001t0001g0164others(4): Show | 7 | HG02622.hp1 HG03669.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2292_64-2280dup others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | ||||||
| chr1:155971706
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64-2406C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971706 | ||||||
| chr1:155971789
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.64-2489A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971789 | ||||||
| chr1:155971842
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.64-2542C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971842 | ||||||
| chr1:155971883
|
T | TAAAAAAA others(4): Show |
1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2594_64-2584dup others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971883 | ||||||
| chr1:155971894
|
A | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.64-2594T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971894 | ||||||
| chr1:155971902
|
C | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2602G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971902 | ||||||
| chr1:155971904
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.64-2604A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971904 | ||||||
| chr1:155971912
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0030others(3): Show | 10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2612A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971912 | ||||||
| chr1:155971914
|
T | C | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2614A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971914 | ||||||
| chr1:155972080
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.64-2780A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972080 | ||||||
| chr1:155972184
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64-2884A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972184 | ||||||
| chr1:155972904
|
A | G | 12 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-3604T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972904 | ||||||
| chr1:155973003
|
A | C | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-3703T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973003 | ||||||
| chr1:155973488
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-4188T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973488 | ||||||
| chr1:155973517
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02015.hp1 HG02083.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4217C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973517 | ||||||
| chr1:155973659
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.64-4359A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973659 | ||||||
| chr1:155973732
|
C | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-4432G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973732 | ||||||
| chr1:155974398
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(95): Show | 120 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+3967A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974398 | ||||||
| chr1:155974524
|
C | T | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+3841G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974524 | ||||||
| chr1:155974552
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+3813C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974552 | ||||||
| chr1:155974587
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.63+3778C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974587 | ||||||
| chr1:155974835
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0022others(19): Show | 27 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.63+3530C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974835 | ||||||
| chr1:155974852
|
A | AG | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(69): Show | 89 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.63+3512dupC | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974852 | ||||||
| chr1:155974979
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.63+3386G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974979 | ||||||
| chr1:155975073
|
A | G | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+3292T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975073 | ||||||
| chr1:155975210
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 5 | HG01891.hp1 HG02145.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3155G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975210 | ||||||
| chr1:155975567
|
C | G | 1 | a0001c0007t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+2798G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975567 | ||||||
| chr1:155975618
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+2747G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975618 | ||||||
| chr1:155976224
|
C | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG00280.hp2 HG01074.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2141G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976224 | ||||||
| chr1:155976382
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.63+1983G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976382 | ||||||
| chr1:155976608
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(96): Show | 121 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+1757T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976608 | ||||||
| chr1:155976750
|
A | C | 1 | a0001c0001t0006g0106 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.63+1615T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976750 | ||||||
| chr1:155977635
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+730T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977635 | ||||||
| chr1:155977742
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0030others(3): Show | 10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+623C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977742 | ||||||
| chr1:155977844
|
G | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG00099.hp1 HG01168.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+521C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977844 | ||||||
| chr1:155977884
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0030others(3): Show | 10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+481G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977884 | ||||||
| chr1:155977907
|
C | T | 1 | a0001c0001t0001g0011 | 2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.63+458G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977907 | ||||||
| chr1:155978009
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.63+356C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978009 | ||||||
| chr1:155978084
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(84): Show | 105 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.63+281T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978084 | ||||||
| chr1:155978139
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(89): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.63+226G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978139 | ||||||
| chr1:155978187
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+178G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978187 |