Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79033 |
|---|---|
| ensemblid | ENSG00000117419.16 |
| hgncid | 17276 |
| symbol | ERI3 |
| name | ERI1 exoribonuclease family member 3 |
| refseq_nuc | NM_024066.3 |
| refseq_prot | NP_076971.1 |
| ensembl_nuc | ENST00000372257.7 |
| ensembl_prot | ENSP00000361331.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 44221070 |
| end | 44355257 |
| strand | - |
| ver | v1.2 |
| region | chr1:44221070-44355257 |
| region5000 | chr1:44216070-44360257 |
| regionname0 | ERI3_chr1_44221070_44355257 |
| regionname5000 | ERI3_chr1_44216070_44360257 |
| 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 | 337 | 340 | 86 | 60 | 154 | 8 | 30 | 116 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| 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 | 1014 | 337 | 84 | 60 | 153 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| c0002 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| c0003 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| c0004 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| 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 | 720 | 333 | 81 | 60 | 152 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| t0002 | 0/0 | 720 | 3 | 3 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| t0003 | 0/0 | 720 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| t0004 | 0/0 | 720 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| t0005 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| t0006 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0333 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| 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 | 1014 | 337 | 84 | 60 | 153 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0002 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0003 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0004 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1733 | 330 | 79 | 60 | 151 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0001t0002 | 0/0 | 1733 | 3 | 3 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0001t0003 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0001t0004 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0001t0005 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0001t0006 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0002t0001 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0003t0001 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| a0001c0004t0001 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | copy fasta | chr1 | 44216070 | 44360257 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0333 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0001t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0340 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0258 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ASW | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ASW | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | GIH | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0138 | REF | REF | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0333 | REF | REF | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44221564
|
C | T | 1 | a0001c0002 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1008G>A | p.Pro336Pro | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 1239/1733 | 1008/1014 | 336/337 | chr1 | 44221564 | ||
| chr1:44308357
|
G | A | 1 | a0001c0003 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.711C>T | p.Asn237Asn | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/9 | 942/1733 | 711/1014 | 237/337 | chr1 | 44308357 | ||
| chr1:44319721
|
T | C | 1 | a0001c0004 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.513A>G | p.Leu171Leu | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/9 | 744/1733 | 513/1014 | 171/337 | chr1 | 44319721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44221123
|
G | A | 1 | a0001c0001t0004 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 435 | chr1 | 44221123 | |||||
| chr1:44221232
|
G | C | 1 | a0001c0001t0002 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 326 | chr1 | 44221232 | |||||
| chr1:44221284
|
C | A | 1 | a0001c0001t0005 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 274 | chr1 | 44221284 | |||||
| chr1:44221365
|
C | T | 1 | a0001c0001t0003 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 193 | chr1 | 44221365 | |||||
| chr1:44355222
|
G | A | 1 | a0001c0001t0006 | 1 | HG02572.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-196C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/9 | chr1 | 44355222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44221880
|
C | T | 19 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(16): Show | 19 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.932-240G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44221880 | ||||||
| chr1:44221885
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-245A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44221885 | ||||||
| chr1:44222242
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.932-602T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222242 | ||||||
| chr1:44222366
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-726G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222366 | ||||||
| chr1:44222434
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.932-794G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222434 | ||||||
| chr1:44222570
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.932-930A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222570 | ||||||
| chr1:44222604
|
G | C | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-964C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222604 | ||||||
| chr1:44222607
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.932-967C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222607 | ||||||
| chr1:44222749
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.932-1109G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222749 | ||||||
| chr1:44222857
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-1217C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222857 | ||||||
| chr1:44222891
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.932-1251G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222891 | ||||||
| chr1:44223015
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.932-1375G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223015 | ||||||
| chr1:44223198
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.932-1558C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223198 | ||||||
| chr1:44223209
|
C | T | 4 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0297others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1569G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223209 | ||||||
| chr1:44223217
|
G | A | 16 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-1577C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223217 | ||||||
| chr1:44223243
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.932-1603G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223243 | ||||||
| chr1:44223311
|
G | C | 1 | a0001c0002t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.932-1671C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223311 | ||||||
| chr1:44223444
|
A | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0297a0001c0001t0001g0299 | 3 | HG02109.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.932-1804T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223444 | ||||||
| chr1:44223534
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0164others(1): Show | 4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1894A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223534 | ||||||
| chr1:44223578
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.932-1938C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223578 | ||||||
| chr1:44223621
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-1981A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223621 | ||||||
| chr1:44223763
|
C | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-2123G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223763 | ||||||
| chr1:44223789
|
T | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.932-2149A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223789 | ||||||
| chr1:44223825
|
C | T | 16 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-2185G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223825 | ||||||
| chr1:44223934
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.932-2294A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223934 | ||||||
| chr1:44223937
|
A | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-2297T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223937 | ||||||
| chr1:44223955
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.932-2315T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223955 | ||||||
| chr1:44223960
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.932-2320C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223960 | ||||||
| chr1:44224317
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.932-2677G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224317 | ||||||
| chr1:44224484
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0203 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-2844G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224484 | ||||||
| chr1:44224496
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0145 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-2856T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224496 | ||||||
| chr1:44225380
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-3740C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225380 | ||||||
| chr1:44225464
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.932-3824T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225464 | ||||||
| chr1:44225663
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.932-4023G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225663 | ||||||
| chr1:44225663
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-4023G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225663 | ||||||
| chr1:44225860
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.932-4220T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225860 | ||||||
| chr1:44226534
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.932-4894A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226534 | ||||||
| chr1:44226676
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-5036A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226676 | ||||||
| chr1:44226741
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.932-5101A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226741 | ||||||
| chr1:44226778
|
A | AAC | 18 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(15): Show | 18 | HG00621.hp2 HG00738.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.932-5140_932-5139d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACAC | 39 | a0001c0001t0001g0092a0001c0001t0001g0122a0001c0001t0001g0123others(36): Show | 39 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.932-5142_932-5139d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACAC | 45 | a0001c0001t0001g0117a0001c0001t0001g0205a0001c0001t0001g0209others(42): Show | 45 | HG00438.hp2 HG00544.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.932-5144_932-5139d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACACA others(1): Show |
55 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0151others(52): Show | 55 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.932-5146_932-5139d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACACA others(3): Show |
22 | a0001c0001t0001g0125a0001c0001t0001g0149a0001c0001t0001g0154others(19): Show | 22 | HG00673.hp2 HG01978.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.932-5148_932-5139d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACACA others(5): Show |
6 | a0001c0001t0001g0097a0001c0001t0001g0157a0001c0001t0001g0198others(3): Show | 6 | HG00639.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-5150_932-5139d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACACA others(7): Show |
1 | a0001c0001t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.932-5152_932-5139d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
A | AACACACA others(9): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0115 | 2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.932-5154_932-5139d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
AAC | A | 24 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(21): Show | 24 | HG00280.hp1 HG00280.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.932-5140_932-5139d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226778
|
AACAC | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0121a0001c0001t0001g0127others(23): Show | 26 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.932-5142_932-5139d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | ||||||
| chr1:44226816
|
A | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.932-5176T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226816 | ||||||
| chr1:44227113
|
C | T | 90 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0231others(87): Show | 90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.932-5473G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227113 | ||||||
| chr1:44227200
|
C | T | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-5560G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227200 | ||||||
| chr1:44227474
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.932-5834C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227474 | ||||||
| chr1:44227558
|
AT | A | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.932-5919delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227558 | ||||||
| chr1:44227574
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-5934T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227574 | ||||||
| chr1:44227753
|
C | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0238a0001c0001t0001g0300others(1): Show | 4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-6113G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227753 | ||||||
| chr1:44228043
|
A | G | 141 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.932-6403T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228043 | ||||||
| chr1:44228093
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.932-6453C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228093 | ||||||
| chr1:44228111
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.932-6471C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228111 | ||||||
| chr1:44228301
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0219 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.932-6661C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228301 | ||||||
| chr1:44228682
|
A | G | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.932-7042T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228682 | ||||||
| chr1:44228804
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0107others(1): Show | 4 | HG01261.hp1 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-7164C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228804 | ||||||
| chr1:44228918
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.932-7278C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228918 | ||||||
| chr1:44228991
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.932-7351G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228991 | ||||||
| chr1:44229205
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0006g0340 | 3 | HG00642.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.932-7565C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229205 | ||||||
| chr1:44229509
|
C | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.932-7869G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229509 | ||||||
| chr1:44229618
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.932-7978C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229618 | ||||||
| chr1:44229632
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.932-7992C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229632 | ||||||
| chr1:44229642
|
T | C | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.932-8002A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229642 | ||||||
| chr1:44229650
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.932-8010G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229650 | ||||||
| chr1:44229690
|
G | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-8050C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229690 | ||||||
| chr1:44229698
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-8058C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229698 | ||||||
| chr1:44229751
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.932-8111C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229751 | ||||||
| chr1:44229770
|
A | AC | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.932-8131dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229770 | ||||||
| chr1:44229796
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.932-8156G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229796 | ||||||
| chr1:44229928
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-8288G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229928 | ||||||
| chr1:44229985
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.932-8345G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229985 | ||||||
| chr1:44229986
|
G | A | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-8346C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229986 | ||||||
| chr1:44230116
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.932-8476T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230116 | ||||||
| chr1:44230185
|
A | G | 12 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-8545T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230185 | ||||||
| chr1:44230273
|
C | T | 12 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-8633G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230273 | ||||||
| chr1:44230301
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.932-8661T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230301 | ||||||
| chr1:44230316
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.932-8676G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230316 | ||||||
| chr1:44230495
|
G | T | 33 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0132others(30): Show | 33 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8855C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230495 | ||||||
| chr1:44230610
|
C | T | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.932-8970G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230610 | ||||||
| chr1:44231379
|
C | T | 3 | a0001c0001t0001g0332a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG01167.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.932-9739G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231379 | ||||||
| chr1:44231583
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.932-9943C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231583 | ||||||
| chr1:44231642
|
G | A | 1 | a0001c0003t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.932-10002C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231642 | ||||||
| chr1:44231669
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.932-10029G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231669 | ||||||
| chr1:44231764
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-10124G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231764 | ||||||
| chr1:44231844
|
C | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0081 | 2 | HG00423.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.932-10204G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231844 | ||||||
| chr1:44232001
|
A | T | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-10361T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232001 | ||||||
| chr1:44232065
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.932-10425C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232065 | ||||||
| chr1:44232084
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.932-10444G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232084 | ||||||
| chr1:44232499
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0086 | 2 | HG00621.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.932-10859T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232499 | ||||||
| chr1:44232536
|
ACTT | A | 16 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-10899_932-1089 others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232536 | ||||||
| chr1:44232813
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.932-11173G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232813 | ||||||
| chr1:44232917
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.932-11277A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232917 | ||||||
| chr1:44232924
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-11284C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232924 | ||||||
| chr1:44233401
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.932-11761G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233401 | ||||||
| chr1:44233405
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.932-11765G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233405 | ||||||
| chr1:44233405
|
C | CT | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0173others(3): Show | 6 | HG01167.hp1 HG02040.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-11766dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233405 | ||||||
| chr1:44233507
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.932-11867C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233507 | ||||||
| chr1:44233684
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.932-12044A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233684 | ||||||
| chr1:44233882
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.932-12242C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233882 | ||||||
| chr1:44234010
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0112 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.932-12370C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234010 | ||||||
| chr1:44234176
|
T | G | 90 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0231others(87): Show | 90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.932-12536A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234176 | ||||||
| chr1:44234190
|
CCAATAAT others(30): Show |
C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-12587_932-1255 others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234190 | ||||||
| chr1:44234440
|
A | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-12800T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234440 | ||||||
| chr1:44234632
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.932-12992G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234632 | ||||||
| chr1:44234852
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0044others(2): Show | 5 | NA18962.hp2 NA18971.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+13087G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234852 | ||||||
| chr1:44235118
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.931+12821C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235118 | ||||||
| chr1:44235468
|
C | T | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+12471G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235468 | ||||||
| chr1:44235533
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+12406A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235533 | ||||||
| chr1:44235542
|
G | T | 1 | a0001c0001t0006g0340 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.931+12397C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235542 | ||||||
| chr1:44235605
|
C | G | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.931+12334G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235605 | ||||||
| chr1:44235745
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+12194A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235745 | ||||||
| chr1:44236185
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.931+11754G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236185 | ||||||
| chr1:44236256
|
T | C | 12 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+11683A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236256 | ||||||
| chr1:44236268
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0193 | 2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.931+11671G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236268 | ||||||
| chr1:44236580
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+11359C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236580 | ||||||
| chr1:44236907
|
G | A | 11 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0143others(8): Show | 11 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+11032C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236907 | ||||||
| chr1:44236951
|
C | T | 95 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(92): Show | 95 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.931+10988G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236951 | ||||||
| chr1:44237043
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+10896C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237043 | ||||||
| chr1:44237231
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.931+10708A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237231 | ||||||
| chr1:44237637
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.931+10302G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237637 | ||||||
| chr1:44237704
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.931+10235G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237704 | ||||||
| chr1:44237706
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.931+10233C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237706 | ||||||
| chr1:44237707
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.931+10232T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237707 | ||||||
| chr1:44238036
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+9903T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238036 | ||||||
| chr1:44238196
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+9743G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238196 | ||||||
| chr1:44238277
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.931+9662C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238277 | ||||||
| chr1:44238358
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.931+9581T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238358 | ||||||
| chr1:44238372
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9567G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238372 | ||||||
| chr1:44238531
|
G | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0147a0001c0001t0001g0150others(3): Show | 6 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9408C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238531 | ||||||
| chr1:44238569
|
C | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9370G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238569 | ||||||
| chr1:44238636
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.931+9303G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238636 | ||||||
| chr1:44238755
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.931+9184T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238755 | ||||||
| chr1:44239039
|
C | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+8900G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239039 | ||||||
| chr1:44239104
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | NA18965.hp2 NA18981.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+8835C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239104 | ||||||
| chr1:44239226
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931+8713C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239226 | ||||||
| chr1:44239270
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+8669T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239270 | ||||||
| chr1:44239550
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.931+8389G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239550 | ||||||
| chr1:44239716
|
C | G | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.931+8223G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239716 | ||||||
| chr1:44239782
|
A | AAGAGGAG others(2): Show |
4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+8148_931+8156d others(11): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239782 | ||||||
| chr1:44240013
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG02572.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.931+7926G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240013 | ||||||
| chr1:44240127
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.931+7812C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240127 | ||||||
| chr1:44240159
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.931+7780C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240159 | ||||||
| chr1:44240330
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.931+7609C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240330 | ||||||
| chr1:44240440
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.931+7499C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240440 | ||||||
| chr1:44240441
|
C | T | 16 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.931+7498G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240441 | ||||||
| chr1:44241396
|
T | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.931+6543A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241396 | ||||||
| chr1:44241534
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+6405G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241534 | ||||||
| chr1:44241556
|
C | G | 1 | a0001c0001t0006g0340 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.931+6383G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241556 | ||||||
| chr1:44241608
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.931+6331C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241608 | ||||||
| chr1:44241623
|
G | C | 249 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0090others(246): Show | 249 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.931+6316C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241623 | ||||||
| chr1:44241739
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.931+6200G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241739 | ||||||
| chr1:44241805
|
C | CACAT | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 172 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.931+6130_931+6133d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | ||||||
| chr1:44241805
|
C | CACATACA others(1): Show |
22 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0124others(19): Show | 22 | HG00280.hp1 HG00438.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+6126_931+6133d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | ||||||
| chr1:44241805
|
C | CACATACA others(5): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0170a0001c0001t0001g0263 | 3 | HG00423.hp2 HG01884.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.931+6122_931+6133d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | ||||||
| chr1:44241805
|
CACAT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(52): Show | 55 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.931+6130_931+6133d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | ||||||
| chr1:44241805
|
CACATACA others(5): Show |
C | 2 | a0001c0001t0001g0302a0001c0004t0001g0258 | 2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.931+6122_931+6133d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | ||||||
| chr1:44241866
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG01255.hp2 HG01517.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.931+6073G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241866 | ||||||
| chr1:44241963
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.931+5976G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241963 | ||||||
| chr1:44242096
|
G | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.931+5843C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242096 | ||||||
| chr1:44242256
|
G | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0209 | 2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.931+5683C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242256 | ||||||
| chr1:44242320
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.931+5619G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242320 | ||||||
| chr1:44242373
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.931+5566T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242373 | ||||||
| chr1:44242473
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.931+5466G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242473 | ||||||
| chr1:44242618
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.931+5321C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242618 | ||||||
| chr1:44242694
|
A | AC | 5 | a0001c0001t0001g0056a0001c0001t0001g0129a0001c0001t0001g0167others(2): Show | 5 | HG01433.hp2 HG02145.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+5244dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242694 | ||||||
| chr1:44242711
|
A | G | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.931+5228T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242711 | ||||||
| chr1:44242796
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.931+5143C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242796 | ||||||
| chr1:44242934
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.931+5005C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242934 | ||||||
| chr1:44243233
|
AC | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+4705delG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243233 | ||||||
| chr1:44243314
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+4625C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243314 | ||||||
| chr1:44243546
|
G | A | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.931+4393C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243546 | ||||||
| chr1:44243752
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0001g0188a0001c0001t0001g0191others(4): Show | 7 | HG00621.hp1 HG02738.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+4187G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243752 | ||||||
| chr1:44243773
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+4166G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243773 | ||||||
| chr1:44244125
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.931+3814A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244125 | ||||||
| chr1:44244385
|
A | G | 141 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.931+3554T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244385 | ||||||
| chr1:44244421
|
C | T | 71 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.931+3518G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244421 | ||||||
| chr1:44244559
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.931+3380C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244559 | ||||||
| chr1:44244692
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+3247C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244692 | ||||||
| chr1:44244811
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.931+3128G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244811 | ||||||
| chr1:44245097
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+2842C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245097 | ||||||
| chr1:44245151
|
C | T | 106 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(103): Show | 106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.931+2788G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245151 | ||||||
| chr1:44245624
|
T | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00544.hp2 HG01167.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+2315A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245624 | ||||||
| chr1:44245709
|
T | C | 140 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.931+2230A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245709 | ||||||
| chr1:44245719
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+2220T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245719 | ||||||
| chr1:44245745
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.931+2194T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245745 | ||||||
| chr1:44245924
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.931+2015A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245924 | ||||||
| chr1:44246252
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.931+1687A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246252 | ||||||
| chr1:44246425
|
G | A | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+1514C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246425 | ||||||
| chr1:44246434
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.931+1505C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246434 | ||||||
| chr1:44246485
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+1454G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246485 | ||||||
| chr1:44246613
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1326A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246613 | ||||||
| chr1:44246747
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.931+1192A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246747 | ||||||
| chr1:44246799
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.931+1140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246799 | ||||||
| chr1:44246898
|
C | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+1041G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246898 | ||||||
| chr1:44246899
|
C | A | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.931+1040G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246899 | ||||||
| chr1:44247398
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+541G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247398 | ||||||
| chr1:44247471
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.931+468G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247471 | ||||||
| chr1:44247641
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.931+298A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247641 | ||||||
| chr1:44247795
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.931+144G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247795 | ||||||
| chr1:44248128
|
T | C | 1 | a0001c0001t0001g0324 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.832-90A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248128 | ||||||
| chr1:44248310
|
C | T | 16 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-272G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248310 | ||||||
| chr1:44248396
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.832-358G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248396 | ||||||
| chr1:44248702
|
A | AGT | 12 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0065others(9): Show | 12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-666_832-665dup others(2): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | ||||||
| chr1:44248702
|
A | AGTGTGTG others(1): Show |
59 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0124others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.832-672_832-665dup others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | ||||||
| chr1:44248702
|
A | AGTGTGTG others(3): Show |
46 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0132others(43): Show | 46 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.832-674_832-665dup others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | ||||||
| chr1:44248702
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0337 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.832-676_832-665dup others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | ||||||
| chr1:44248702
|
AGT | A | 3 | a0001c0001t0001g0292a0001c0001t0001g0332a0001c0001t0001g0334 | 3 | HG01167.hp1 HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.832-666_832-665del others(2): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | ||||||
| chr1:44248882
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.832-844G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248882 | ||||||
| chr1:44248932
|
G | GC | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-895_832-894ins others(1): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248932 | ||||||
| chr1:44248960
|
G | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-922C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248960 | ||||||
| chr1:44249220
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-1182C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249220 | ||||||
| chr1:44249325
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1287C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249325 | ||||||
| chr1:44249580
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-1542T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249580 | ||||||
| chr1:44249874
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-1836G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249874 | ||||||
| chr1:44249930
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.832-1892G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249930 | ||||||
| chr1:44249948
|
G | A | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.832-1910C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249948 | ||||||
| chr1:44249960
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-1922A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249960 | ||||||
| chr1:44249989
|
G | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(3): Show | 6 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-1951C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249989 | ||||||
| chr1:44250165
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0158 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2127A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250165 | ||||||
| chr1:44250202
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2164C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250202 | ||||||
| chr1:44250268
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-2230A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250268 | ||||||
| chr1:44250299
|
G | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0158 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2261C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250299 | ||||||
| chr1:44250476
|
G | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0158 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2438C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250476 | ||||||
| chr1:44250529
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.832-2491C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250529 | ||||||
| chr1:44250658
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.832-2620T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250658 | ||||||
| chr1:44250734
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.832-2696C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250734 | ||||||
| chr1:44250928
|
C | T | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-2890G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250928 | ||||||
| chr1:44250939
|
C | G | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-2901G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250939 | ||||||
| chr1:44250957
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832-2919G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250957 | ||||||
| chr1:44251193
|
A | AC | 6 | a0001c0001t0001g0056a0001c0001t0001g0089a0001c0001t0001g0104others(3): Show | 6 | HG00438.hp2 HG01261.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-3156dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251193 | ||||||
| chr1:44251229
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.832-3191G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251229 | ||||||
| chr1:44251239
|
G | A | 3 | a0001c0001t0001g0332a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG01167.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.832-3201C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251239 | ||||||
| chr1:44251337
|
G | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.832-3299C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251337 | ||||||
| chr1:44251586
|
G | A | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-3548C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251586 | ||||||
| chr1:44251597
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-3559T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251597 | ||||||
| chr1:44251778
|
T | C | 141 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.832-3740A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251778 | ||||||
| chr1:44251904
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.832-3866C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251904 | ||||||
| chr1:44251932
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-3894C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251932 | ||||||
| chr1:44251980
|
C | T | 87 | a0001c0001t0001g0157a0001c0001t0001g0227a0001c0001t0001g0228others(84): Show | 87 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.832-3942G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251980 | ||||||
| chr1:44252247
|
G | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4209C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252247 | ||||||
| chr1:44252390
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-4352A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252390 | ||||||
| chr1:44252627
|
C | T | 24 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0147others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-4589G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252627 | ||||||
| chr1:44253066
|
G | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.832-5028C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253066 | ||||||
| chr1:44253581
|
C | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | NA18959.hp1 NA18970.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-5543G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253581 | ||||||
| chr1:44253709
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.832-5671T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253709 | ||||||
| chr1:44253718
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.832-5680C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253718 | ||||||
| chr1:44254249
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.832-6211A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254249 | ||||||
| chr1:44254409
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.832-6371T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254409 | ||||||
| chr1:44254657
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.832-6619G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254657 | ||||||
| chr1:44255034
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-6996A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255034 | ||||||
| chr1:44255311
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.832-7273A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255311 | ||||||
| chr1:44255315
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.832-7277A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255315 | ||||||
| chr1:44255319
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.832-7281A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255319 | ||||||
| chr1:44255562
|
A | C | 10 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(7): Show | 10 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-7524T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255562 | ||||||
| chr1:44255747
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0006g0340 | 3 | HG00642.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.832-7709G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255747 | ||||||
| chr1:44255803
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.832-7765A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255803 | ||||||
| chr1:44255830
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.832-7792A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255830 | ||||||
| chr1:44256067
|
G | A | 110 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0035others(107): Show | 110 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.832-8029C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256067 | ||||||
| chr1:44256215
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-8177G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256215 | ||||||
| chr1:44256796
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.832-8758C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256796 | ||||||
| chr1:44257165
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.832-9127G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44257165 | ||||||
| chr1:44257274
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.832-9236A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44257274 | ||||||
| chr1:44258072
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832-10034C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258072 | ||||||
| chr1:44258215
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.832-10177T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258215 | ||||||
| chr1:44258350
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-10312G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258350 | ||||||
| chr1:44258530
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0006g0340 | 2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832-10492G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258530 | ||||||
| chr1:44258543
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-10505A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258543 | ||||||
| chr1:44258640
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.832-10602G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258640 | ||||||
| chr1:44258672
|
G | C | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-10634C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258672 | ||||||
| chr1:44258906
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-10868G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258906 | ||||||
| chr1:44258961
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832-10923G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258961 | ||||||
| chr1:44259064
|
T | G | 12 | a0001c0001t0001g0059a0001c0001t0001g0134a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-11026A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259064 | ||||||
| chr1:44259106
|
C | T | 139 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.832-11068G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259106 | ||||||
| chr1:44259116
|
A | G | 79 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.832-11078T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259116 | ||||||
| chr1:44259340
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.832-11302C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259340 | ||||||
| chr1:44259558
|
C | T | 7 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-11520G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259558 | ||||||
| chr1:44259640
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.832-11602C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259640 | ||||||
| chr1:44259681
|
A | AACAC | 3 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0045 | 3 | NA18943.hp1 NA18951.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.832-11647_832-1164 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259681 | ||||||
| chr1:44259689
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0045others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-11651C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GAC | 22 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0036others(19): Show | 22 | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.832-11653_832-1165 others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACAC | 3 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0336 | 3 | HG00642.hp2 HG02717.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.832-11655_832-1165 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACAC | 33 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(30): Show | 33 | HG00642.hp1 HG01169.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.832-11657_832-1165 others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(1): Show |
37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.832-11659_832-1165 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(3): Show |
23 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0028others(20): Show | 23 | HG00544.hp1 HG01167.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.832-11661_832-1165 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(5): Show |
29 | a0001c0001t0001g0059a0001c0001t0001g0118a0001c0001t0001g0134others(26): Show | 29 | HG00738.hp1 HG01516.hp2 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.832-11663_832-1165 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(7): Show |
53 | a0001c0001t0001g0033a0001c0001t0001g0101a0001c0001t0001g0107others(50): Show | 53 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.832-11665_832-1165 others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(9): Show |
31 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0102others(28): Show | 31 | HG00280.hp2 HG00733.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-11667_832-1165 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(11): Show |
15 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0103others(12): Show | 15 | HG01884.hp1 HG01978.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-11669_832-1165 others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(13): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0120others(1): Show | 4 | HG02027.hp2 HG03139.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-11671_832-1165 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(15): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0204a0001c0001t0001g0221 | 3 | HG02622.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.832-11673_832-1165 others(26): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(17): Show |
1 | a0001c0001t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.832-11675_832-1165 others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
G | GACACACA others(9): Show |
4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-11652_832-1165 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259689
|
GACACAC | G | 67 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(64): Show | 67 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.832-11657_832-1165 others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | ||||||
| chr1:44259724
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832-11687_832-1168 others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | ||||||
| chr1:44259724
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.832-11687_832-1168 others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | ||||||
| chr1:44259724
|
A | ACACACAC others(12): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0111 | 2 | HG01261.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.832-11687_832-1168 others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | ||||||
| chr1:44259871
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.832-11833G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259871 | ||||||
| chr1:44259875
|
C | CTAGA | 72 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(69): Show | 72 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.832-11841_832-1183 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
C | CTAGATAG others(1): Show |
27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0030others(24): Show | 27 | HG00423.hp2 HG00673.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.832-11845_832-1183 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
C | CTAGATAG others(5): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0279 | 2 | HG02004.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.832-11849_832-1183 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
C | CTAGATAG others(9): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0307 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.832-11853_832-1183 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
C | CTAGATAG others(21): Show |
1 | a0001c0001t0001g0014 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.832-11865_832-1183 others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
CTAGA | C | 9 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0177others(6): Show | 9 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-11841_832-1183 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
CTAGATAG others(1): Show |
C | 6 | a0001c0001t0001g0089a0001c0001t0001g0109a0001c0001t0001g0115others(3): Show | 6 | HG00642.hp1 HG01255.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-11845_832-1183 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259875
|
CTAGATAG others(5): Show |
C | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.832-11849_832-1183 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | ||||||
| chr1:44259876
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.832-11838A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259876 | ||||||
| chr1:44259912
|
T | C | 10 | a0001c0001t0001g0134a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-11874A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259912 | ||||||
| chr1:44259912
|
T | TAGAC | 4 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-11875_832-1187 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259912 | ||||||
| chr1:44259916
|
T | C | 16 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0166others(13): Show | 16 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-11878A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | ||||||
| chr1:44259916
|
T | TAGAC | 8 | a0001c0001t0001g0140a0001c0001t0001g0160a0001c0001t0001g0208others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-11879_832-1187 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | ||||||
| chr1:44259916
|
T | TAGACAGA others(1): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0334a0001c0001t0001g0339 | 3 | HG01261.hp2 NA19056.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.832-11879_832-1187 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | ||||||
| chr1:44259916
|
T | TAGACAGA others(5): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0204a0001c0001t0001g0206 | 3 | HG02622.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.832-11879_832-1187 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | ||||||
| chr1:44259920
|
T | C | 58 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0097others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.832-11882A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGAC | 37 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0100others(34): Show | 37 | HG00558.hp2 HG01071.hp1 HG01978.hp2 others(34): Show |
intron_variant | MODIFIER | c.832-11886_832-1188 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGACAGA others(5): Show |
6 | a0001c0001t0001g0145a0001c0001t0001g0164a0001c0001t0001g0205others(3): Show | 6 | HG02976.hp2 HG03041.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-11894_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGACAGA others(9): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.832-11898_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(1): Show |
18 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0060others(15): Show | 18 | HG00438.hp1 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(5): Show |
11 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101others(8): Show | 11 | HG00280.hp2 HG01261.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(13): Show |
1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.832-11883_832-1188 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(5): Show |
7 | a0001c0001t0001g0020a0001c0001t0001g0073a0001c0001t0001g0252others(4): Show | 7 | HG01516.hp2 HG01517.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(9): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0289 | 2 | HG00738.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.832-11883_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(9): Show |
2 | a0001c0001t0001g0268a0001c0001t0001g0311 | 2 | HG03704.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.832-11883_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
T | TAGATAGA others(13): Show |
1 | a0001c0001t0001g0266 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.832-11883_832-1188 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259920
|
TAGAC | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0301 | 3 | HG00408.hp1 HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.832-11886_832-1188 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | ||||||
| chr1:44259924
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0085a0001c0001t0001g0116others(4): Show | 7 | HG00733.hp2 HG02027.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-11886G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259924 | ||||||
| chr1:44259980
|
T | C | 9 | a0001c0001t0001g0247a0001c0001t0001g0266a0001c0001t0001g0276others(6): Show | 9 | HG01358.hp2 HG01496.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-11942A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259980 | ||||||
| chr1:44260211
|
T | C | 247 | a0001c0001t0001g0033a0001c0001t0001g0059a0001c0001t0001g0094others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.832-12173A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260211 | ||||||
| chr1:44260244
|
C | G | 140 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.832-12206G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260244 | ||||||
| chr1:44260284
|
G | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-12246C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260284 | ||||||
| chr1:44260348
|
T | C | 24 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0147others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-12310A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260348 | ||||||
| chr1:44260424
|
C | G | 21 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(18): Show | 21 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-12386G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260424 | ||||||
| chr1:44260682
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.832-12644A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260682 | ||||||
| chr1:44260979
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.832-12941G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260979 | ||||||
| chr1:44260998
|
GTT | G | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.832-12962_832-1296 others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260998 | ||||||
| chr1:44261281
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0164others(1): Show | 4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-13243C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261281 | ||||||
| chr1:44261631
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832-13593C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261631 | ||||||
| chr1:44261769
|
A | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-13731T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261769 | ||||||
| chr1:44261906
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-13868T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261906 | ||||||
| chr1:44261940
|
T | C | 99 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(96): Show | 99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.832-13902A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261940 | ||||||
| chr1:44261999
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0070a0001c0001t0001g0073 | 3 | NA18997.hp1 NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.832-13961C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261999 | ||||||
| chr1:44262124
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.832-14086C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262124 | ||||||
| chr1:44262290
|
C | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0107 | 3 | HG01261.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.832-14252G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262290 | ||||||
| chr1:44262329
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-14291C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262329 | ||||||
| chr1:44262422
|
C | G | 1 | a0001c0001t0003g0010 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.832-14384G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262422 | ||||||
| chr1:44262472
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.832-14434A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262472 | ||||||
| chr1:44262572
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-14534C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262572 | ||||||
| chr1:44262645
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.832-14607C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262645 | ||||||
| chr1:44262759
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-14721C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262759 | ||||||
| chr1:44262892
|
T | C | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-14854A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262892 | ||||||
| chr1:44263076
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.832-15038T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263076 | ||||||
| chr1:44263515
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.832-15477C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263515 | ||||||
| chr1:44263596
|
T | A | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.832-15558A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263596 | ||||||
| chr1:44263606
|
A | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0297others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-15568T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263606 | ||||||
| chr1:44263685
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0165 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.832-15647T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263685 | ||||||
| chr1:44263724
|
C | T | 136 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.832-15686G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263724 | ||||||
| chr1:44264209
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-16171A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264209 | ||||||
| chr1:44264264
|
T | C | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-16226A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264264 | ||||||
| chr1:44264296
|
T | C | 140 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.832-16258A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264296 | ||||||
| chr1:44264331
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-16293G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264331 | ||||||
| chr1:44264411
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.832-16373G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264411 | ||||||
| chr1:44264617
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-16579G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264617 | ||||||
| chr1:44264632
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-16594G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264632 | ||||||
| chr1:44265151
|
G | GGAGA | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 317 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.832-17117_832-1711 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265151 | ||||||
| chr1:44265304
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.832-17266C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265304 | ||||||
| chr1:44265327
|
A | C | 3 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG01261.hp2 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.832-17289T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265327 | ||||||
| chr1:44265351
|
G | A | 33 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0132others(30): Show | 33 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.832-17313C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265351 | ||||||
| chr1:44265396
|
T | G | 140 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.832-17358A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265396 | ||||||
| chr1:44265439
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832-17401G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265439 | ||||||
| chr1:44265456
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-17418G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265456 | ||||||
| chr1:44265587
|
C | T | 24 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0147others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-17549G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265587 | ||||||
| chr1:44265599
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.832-17561G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265599 | ||||||
| chr1:44265653
|
T | TA | 7 | a0001c0001t0001g0089a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-17616dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265653 | ||||||
| chr1:44265707
|
AGAAAT | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-17674_832-1767 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265707 | ||||||
| chr1:44266267
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.832-18229T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266267 | ||||||
| chr1:44266429
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.832-18391T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266429 | ||||||
| chr1:44266506
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.831+18329A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266506 | ||||||
| chr1:44266558
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.831+18277G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266558 | ||||||
| chr1:44266785
|
G | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+18050C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266785 | ||||||
| chr1:44267129
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.831+17706C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267129 | ||||||
| chr1:44267215
|
C | T | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.831+17620G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267215 | ||||||
| chr1:44267383
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0165 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.831+17452T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267383 | ||||||
| chr1:44267433
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.831+17402C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267433 | ||||||
| chr1:44267492
|
C | T | 1 | a0001c0003t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.831+17343G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267492 | ||||||
| chr1:44267535
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0158 | 2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.831+17300G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267535 | ||||||
| chr1:44267579
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG02572.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+17256G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267579 | ||||||
| chr1:44267644
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.831+17191T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267644 | ||||||
| chr1:44267659
|
TCTGCCTG others(12): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.831+17157_831+1717 others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267659 | ||||||
| chr1:44267720
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.831+17115T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267720 | ||||||
| chr1:44267775
|
T | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0231a0001c0001t0001g0232others(8): Show | 11 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+17060A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267775 | ||||||
| chr1:44267799
|
A | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+17036T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267799 | ||||||
| chr1:44267809
|
G | A | 1 | a0001c0001t0001g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.831+17026C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267809 | ||||||
| chr1:44267916
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+16919G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267916 | ||||||
| chr1:44268269
|
A | AGGACTTC others(3): Show |
138 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.831+16565_831+1656 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44268269 | ||||||
| chr1:44268988
|
G | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15847C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44268988 | ||||||
| chr1:44269220
|
G | A | 27 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(24): Show | 27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.831+15615C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269220 | ||||||
| chr1:44269523
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15312G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269523 | ||||||
| chr1:44269529
|
T | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+15306A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269529 | ||||||
| chr1:44269620
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 4 | NA18962.hp2 NA18971.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15215G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269620 | ||||||
| chr1:44269677
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+15158T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269677 | ||||||
| chr1:44269934
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.831+14901G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269934 | ||||||
| chr1:44269951
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+14884C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269951 | ||||||
| chr1:44270235
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.831+14600G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270235 | ||||||
| chr1:44270300
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.831+14535G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270300 | ||||||
| chr1:44270409
|
C | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+14426G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270409 | ||||||
| chr1:44270649
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+14186A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270649 | ||||||
| chr1:44270945
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.831+13890T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270945 | ||||||
| chr1:44271002
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+13833G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271002 | ||||||
| chr1:44271036
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0219 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.831+13799C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271036 | ||||||
| chr1:44271056
|
C | T | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+13779G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271056 | ||||||
| chr1:44271291
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.831+13544G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271291 | ||||||
| chr1:44271779
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+13056T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271779 | ||||||
| chr1:44272093
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+12742C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272093 | ||||||
| chr1:44272393
|
A | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+12442T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272393 | ||||||
| chr1:44272613
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.831+12222C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272613 | ||||||
| chr1:44272625
|
C | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+12210G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272625 | ||||||
| chr1:44272841
|
A | AAAAAT | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.831+11989_831+1199 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272841
|
A | AAAAATAA others(3): Show |
28 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0241others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+11984_831+1199 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272841
|
A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.831+11979_831+1199 others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272841
|
A | AAAAATAA others(13): Show |
4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11974_831+1199 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272841
|
AAAAAT | A | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(5): Show | 8 | HG01261.hp2 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+11989_831+1199 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272841
|
AAAAATAA others(13): Show |
A | 16 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(13): Show | 16 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+11974_831+1199 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | ||||||
| chr1:44272896
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+11939G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272896 | ||||||
| chr1:44272899
|
T | TA | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+11935dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272899 | ||||||
| chr1:44272929
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11906A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272929 | ||||||
| chr1:44272936
|
T | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.831+11899A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272936 | ||||||
| chr1:44273003
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11832A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273003 | ||||||
| chr1:44273171
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.831+11664G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273171 | ||||||
| chr1:44273306
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+11529G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273306 | ||||||
| chr1:44273370
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0164others(1): Show | 4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11465G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273370 | ||||||
| chr1:44273480
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.831+11355T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273480 | ||||||
| chr1:44273498
|
G | T | 90 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0231others(87): Show | 90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.831+11337C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273498 | ||||||
| chr1:44273669
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.831+11166C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273669 | ||||||
| chr1:44273859
|
G | C | 1 | a0001c0001t0001g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.831+10976C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273859 | ||||||
| chr1:44273861
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG02257.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.831+10974G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273861 | ||||||
| chr1:44274233
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0203 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.831+10602A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274233 | ||||||
| chr1:44274314
|
A | G | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.831+10521T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274314 | ||||||
| chr1:44274334
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+10501C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274334 | ||||||
| chr1:44274352
|
T | C | 246 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(243): Show | 246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.831+10483A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274352 | ||||||
| chr1:44274393
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.831+10442T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274393 | ||||||
| chr1:44274572
|
A | G | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.831+10263T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274572 | ||||||
| chr1:44274764
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.831+10071G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274764 | ||||||
| chr1:44275253
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0152 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.831+9582G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275253 | ||||||
| chr1:44275651
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.831+9184G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275651 | ||||||
| chr1:44275724
|
T | C | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+9111A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275724 | ||||||
| chr1:44275896
|
A | C | 140 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.831+8939T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275896 | ||||||
| chr1:44275917
|
A | AT | 4 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0107others(1): Show | 4 | HG01261.hp1 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+8917dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275917 | ||||||
| chr1:44275986
|
G | A | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0257others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+8849C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275986 | ||||||
| chr1:44276774
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831+8061C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44276774 | ||||||
| chr1:44276888
|
AGG | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7945_831+7946d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44276888 | ||||||
| chr1:44277044
|
G | C | 10 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(7): Show | 10 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+7791C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277044 | ||||||
| chr1:44277247
|
A | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7588T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277247 | ||||||
| chr1:44277308
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+7527G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277308 | ||||||
| chr1:44277310
|
T | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7525A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277310 | ||||||
| chr1:44277473
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+7362T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277473 | ||||||
| chr1:44277479
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.831+7356A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277479 | ||||||
| chr1:44277735
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7100G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277735 | ||||||
| chr1:44277834
|
T | C | 7 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7001A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277834 | ||||||
| chr1:44278132
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+6703C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278132 | ||||||
| chr1:44278375
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+6460C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278375 | ||||||
| chr1:44278425
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+6410G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278425 | ||||||
| chr1:44278477
|
G | GA | 12 | a0001c0001t0001g0021a0001c0001t0001g0089a0001c0001t0001g0109others(9): Show | 12 | HG00642.hp1 HG01081.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+6357dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278477 | ||||||
| chr1:44278477
|
GAA | G | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+6356_831+6357d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278477 | ||||||
| chr1:44278485
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+6350T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278485 | ||||||
| chr1:44278597
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+6238A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278597 | ||||||
| chr1:44278632
|
C | T | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.831+6203G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278632 | ||||||
| chr1:44278693
|
G | A | 15 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.831+6142C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278693 | ||||||
| chr1:44278745
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.831+6090C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278745 | ||||||
| chr1:44278761
|
G | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+6074C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278761 | ||||||
| chr1:44278784
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.831+6051T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278784 | ||||||
| chr1:44278859
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+5976A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278859 | ||||||
| chr1:44279074
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+5761T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279074 | ||||||
| chr1:44279075
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+5760A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279075 | ||||||
| chr1:44279089
|
G | T | 6 | a0001c0001t0001g0332a0001c0001t0001g0334a0001c0001t0001g0335others(3): Show | 6 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+5746C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279089 | ||||||
| chr1:44279186
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+5649T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279186 | ||||||
| chr1:44279217
|
AATAACAC others(24): Show |
A | 5 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0066others(2): Show | 5 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+5587_831+5617d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279217 | ||||||
| chr1:44279230
|
A | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+5605T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279230 | ||||||
| chr1:44279432
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+5403G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279432 | ||||||
| chr1:44279559
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.831+5276G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279559 | ||||||
| chr1:44279778
|
T | A | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.831+5057A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279778 | ||||||
| chr1:44279936
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.831+4899T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279936 | ||||||
| chr1:44279952
|
C | T | 107 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0124others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.831+4883G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279952 | ||||||
| chr1:44280124
|
C | T | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+4711G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280124 | ||||||
| chr1:44280264
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831+4571A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280264 | ||||||
| chr1:44280402
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0066a0001c0001t0001g0072others(1): Show | 4 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+4433C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280402 | ||||||
| chr1:44280438
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.831+4397T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280438 | ||||||
| chr1:44280530
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.831+4305A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280530 | ||||||
| chr1:44280545
|
G | A | 10 | a0001c0001t0001g0227a0001c0001t0001g0252a0001c0001t0001g0268others(7): Show | 10 | HG00738.hp1 HG01256.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+4290C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280545 | ||||||
| chr1:44280781
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.831+4054G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280781 | ||||||
| chr1:44280781
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0006 | 2 | NA18944.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.831+4054G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280781 | ||||||
| chr1:44280880
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.831+3955T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280880 | ||||||
| chr1:44280995
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3840G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280995 | ||||||
| chr1:44281005
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.831+3830T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281005 | ||||||
| chr1:44281212
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.831+3623T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281212 | ||||||
| chr1:44281254
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.831+3581C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281254 | ||||||
| chr1:44281582
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+3253G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281582 | ||||||
| chr1:44281588
|
G | GA | 8 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0229others(5): Show | 8 | HG01081.hp2 HG01175.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+3246dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | ||||||
| chr1:44281588
|
G | GAAA | 8 | a0001c0001t0001g0108a0001c0001t0001g0163a0001c0001t0001g0169others(5): Show | 8 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+3244_831+3246d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | ||||||
| chr1:44281588
|
G | GAAAAA | 6 | a0001c0001t0001g0126a0001c0001t0001g0145a0001c0001t0001g0160others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+3242_831+3246d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | ||||||
| chr1:44281588
|
G | GAAAAAA | 20 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0136others(17): Show | 20 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.831+3241_831+3246d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | ||||||
| chr1:44281599
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0335 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.831+3235_831+3236i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281599 | ||||||
| chr1:44281601
|
A | AAAAAAT | 7 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG00558.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+3233_831+3234i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0334 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.831+3233_831+3234i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AAAT | 9 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0204others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AAATAT | 7 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0148others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AAATATAT | 16 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0149others(13): Show | 16 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG02965.hp1 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.831+3224_831+3233d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | ATATATAT | 7 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0154others(4): Show | 7 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281601
|
A | T | 23 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0075others(20): Show | 23 | HG01071.hp2 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.831+3234T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | ||||||
| chr1:44281602
|
AT | A | 17 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 17 | HG00280.hp2 HG02004.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+3232delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281602 | ||||||
| chr1:44281603
|
T | A | 38 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(35): Show | 38 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.831+3232A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281603 | ||||||
| chr1:44281605
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.831+3230A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281605 | ||||||
| chr1:44281619
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.831+3216A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281619 | ||||||
| chr1:44281639
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.831+3196G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281639 | ||||||
| chr1:44281721
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.831+3114G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281721 | ||||||
| chr1:44281878
|
A | ATG | 45 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0080others(42): Show | 45 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.831+2955_831+2956d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTG | 31 | a0001c0001t0001g0045a0001c0001t0001g0103a0001c0001t0001g0117others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.831+2953_831+2956d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTGTG | 17 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0133others(14): Show | 17 | HG00738.hp1 HG01071.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+2951_831+2956d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0130others(6): Show | 9 | HG01433.hp2 HG01934.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+2949_831+2956d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0154a0001c0001t0001g0176 | 3 | HG01952.hp1 HG01978.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.831+2947_831+2956d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+2945_831+2956d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0189 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.831+2943_831+2956d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.831+2957T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATG | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.831+2955_831+2956d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTG | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0025others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+2953_831+2956d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTG | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG00642.hp2 HG01517.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+2951_831+2956d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTGT others(1): Show |
A | 8 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(5): Show | 8 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+2949_831+2956d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(8): Show | 11 | HG02055.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+2947_831+2956d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTGT others(5): Show |
A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+2945_831+2956d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0275 | 3 | HG01884.hp1 HG02922.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.831+2943_831+2956d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281878
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.831+2941_831+2956d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | ||||||
| chr1:44281926
|
GTA | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0066a0001c0001t0001g0072others(2): Show | 5 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+2907_831+2908d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281926 | ||||||
| chr1:44281928
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG01243.hp2 HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.831+2907T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281928 | ||||||
| chr1:44282300
|
T | C | 247 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0095others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.831+2535A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44282300 | ||||||
| chr1:44282434
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.831+2401C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44282434 | ||||||
| chr1:44283240
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+1595G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283240 | ||||||
| chr1:44283430
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.831+1405A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283430 | ||||||
| chr1:44283464
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.831+1371T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283464 | ||||||
| chr1:44283968
|
C | T | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+867G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283968 | ||||||
| chr1:44283995
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+840G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283995 | ||||||
| chr1:44284209
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+626C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284209 | ||||||
| chr1:44284597
|
G | A | 106 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(103): Show | 106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.831+238C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284597 | ||||||
| chr1:44284817
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.831+18C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284817 | ||||||
| chr1:44285036
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0204a0001c0001t0001g0206 | 3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.759-129A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285036 | ||||||
| chr1:44285121
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.759-214C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285121 | ||||||
| chr1:44285123
|
C | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0138others(3): Show | 6 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-216G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285123 | ||||||
| chr1:44285356
|
G | A | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.759-449C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285356 | ||||||
| chr1:44285381
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.759-474A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285381 | ||||||
| chr1:44285382
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-475A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285382 | ||||||
| chr1:44285534
|
A | G | 107 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0124others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.759-627T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285534 | ||||||
| chr1:44285577
|
C | A | 1 | a0001c0001t0001g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.759-670G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285577 | ||||||
| chr1:44285659
|
C | T | 248 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0094others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.759-752G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285659 | ||||||
| chr1:44285704
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.759-797A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285704 | ||||||
| chr1:44285718
|
G | A | 138 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.759-811C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285718 | ||||||
| chr1:44286038
|
T | C | 107 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0124others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.759-1131A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286038 | ||||||
| chr1:44286278
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.759-1371G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286278 | ||||||
| chr1:44286649
|
C | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0164others(1): Show | 4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-1742G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286649 | ||||||
| chr1:44286897
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.759-1990T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286897 | ||||||
| chr1:44287115
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-2208C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287115 | ||||||
| chr1:44287290
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.759-2383G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287290 | ||||||
| chr1:44287294
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.759-2387A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287294 | ||||||
| chr1:44287333
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.759-2426T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287333 | ||||||
| chr1:44287365
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0043 | 3 | NA18995.hp1 NA19011.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.759-2458G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287365 | ||||||
| chr1:44287431
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.759-2524G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287431 | ||||||
| chr1:44287467
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.759-2560A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287467 | ||||||
| chr1:44287528
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-2621C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287528 | ||||||
| chr1:44287831
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-2924A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287831 | ||||||
| chr1:44287839
|
G | C | 12 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.759-2932C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287839 | ||||||
| chr1:44288016
|
C | T | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.759-3109G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288016 | ||||||
| chr1:44288139
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.759-3232G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288139 | ||||||
| chr1:44288150
|
CCAGA | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.759-3247_759-3244d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288150 | ||||||
| chr1:44288638
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759-3731G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288638 | ||||||
| chr1:44288885
|
T | G | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.759-3978A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288885 | ||||||
| chr1:44288916
|
A | G | 101 | a0001c0001t0001g0052a0001c0001t0001g0110a0001c0001t0001g0221others(98): Show | 101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.759-4009T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288916 | ||||||
| chr1:44288954
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.759-4047G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288954 | ||||||
| chr1:44289045
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759-4138A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289045 | ||||||
| chr1:44289127
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.759-4220C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289127 | ||||||
| chr1:44289342
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.759-4435C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289342 | ||||||
| chr1:44289515
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.759-4608T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289515 | ||||||
| chr1:44289558
|
T | C | 1 | a0001c0001t0005g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.759-4651A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289558 | ||||||
| chr1:44289690
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.759-4783G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289690 | ||||||
| chr1:44289890
|
T | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 233 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.759-4983A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289890 | ||||||
| chr1:44289901
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.759-4994C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289901 | ||||||
| chr1:44289987
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.759-5080A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289987 | ||||||
| chr1:44290100
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.759-5193C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290100 | ||||||
| chr1:44290501
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-5594C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290501 | ||||||
| chr1:44290645
|
G | A | 6 | a0001c0001t0001g0247a0001c0001t0001g0266a0001c0001t0001g0276others(3): Show | 6 | HG01358.hp2 HG01496.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-5738C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290645 | ||||||
| chr1:44290804
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.759-5897C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290804 | ||||||
| chr1:44290874
|
G | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-5967C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290874 | ||||||
| chr1:44290914
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759-6007T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290914 | ||||||
| chr1:44290958
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.759-6051T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290958 | ||||||
| chr1:44290994
|
G | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-6087C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290994 | ||||||
| chr1:44291075
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.759-6168A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291075 | ||||||
| chr1:44291355
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122 | 3 | HG02572.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.759-6448G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291355 | ||||||
| chr1:44291463
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0165 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.759-6556G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291463 | ||||||
| chr1:44291733
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.759-6826C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291733 | ||||||
| chr1:44291753
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-6846A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291753 | ||||||
| chr1:44291806
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.759-6899C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291806 | ||||||
| chr1:44291975
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0297others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-7068C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291975 | ||||||
| chr1:44292365
|
C | T | 10 | a0001c0001t0001g0313a0001c0001t0001g0318a0001c0001t0001g0319others(7): Show | 10 | HG02027.hp1 HG02040.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.759-7458G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292365 | ||||||
| chr1:44292644
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.759-7737C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292644 | ||||||
| chr1:44292708
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.759-7801A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292708 | ||||||
| chr1:44292734
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.759-7827G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292734 | ||||||
| chr1:44293060
|
C | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-8153G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293060 | ||||||
| chr1:44293342
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.759-8435A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293342 | ||||||
| chr1:44293546
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.759-8639G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293546 | ||||||
| chr1:44293547
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.759-8640C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293547 | ||||||
| chr1:44293600
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759-8693G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293600 | ||||||
| chr1:44293716
|
G | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-8809C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293716 | ||||||
| chr1:44293720
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-8813G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293720 | ||||||
| chr1:44293792
|
CCTCA | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0322 | 3 | HG02027.hp1 NA18953.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.759-8889_759-8886d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293792 | ||||||
| chr1:44294027
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.759-9120G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294027 | ||||||
| chr1:44294179
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.759-9272A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294179 | ||||||
| chr1:44294296
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759-9389T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294296 | ||||||
| chr1:44294334
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.759-9427A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294334 | ||||||
| chr1:44294364
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759-9457G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294364 | ||||||
| chr1:44294431
|
C | T | 24 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0147others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.759-9524G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294431 | ||||||
| chr1:44294544
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-9637G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294544 | ||||||
| chr1:44294558
|
T | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-9651A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294558 | ||||||
| chr1:44294763
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.759-9856A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294763 | ||||||
| chr1:44295157
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-10250C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44295157 | ||||||
| chr1:44295878
|
A | G | 105 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(102): Show | 105 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.759-10971T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44295878 | ||||||
| chr1:44296039
|
G | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(23): Show | 26 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.759-11132C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296039 | ||||||
| chr1:44296050
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.759-11143G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296050 | ||||||
| chr1:44296137
|
C | A | 3 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0001g0339 | 3 | HG01261.hp2 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.759-11230G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296137 | ||||||
| chr1:44296138
|
C | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | NA18970.hp1 NA18997.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.759-11231G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296138 | ||||||
| chr1:44296251
|
AG | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0188a0001c0001t0001g0191others(4): Show | 7 | HG00621.hp1 HG02738.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.759-11345delC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296251 | ||||||
| chr1:44296306
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.759-11399G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296306 | ||||||
| chr1:44296486
|
T | A | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.759-11579A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296486 | ||||||
| chr1:44296712
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+11598A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296712 | ||||||
| chr1:44296835
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.758+11475G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296835 | ||||||
| chr1:44296878
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG01243.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.758+11432A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296878 | ||||||
| chr1:44297093
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.758+11217G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297093 | ||||||
| chr1:44297120
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02559.hp1 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+11190G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297120 | ||||||
| chr1:44297130
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.758+11180A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297130 | ||||||
| chr1:44297682
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.758+10628T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297682 | ||||||
| chr1:44297761
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.758+10549A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297761 | ||||||
| chr1:44297993
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 227 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.758+10317C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297993 | ||||||
| chr1:44298592
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.758+9718T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298592 | ||||||
| chr1:44298631
|
C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(5): Show | 8 | NA18939.hp1 NA18941.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.758+9679G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298631 | ||||||
| chr1:44298713
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+9597C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298713 | ||||||
| chr1:44298717
|
C | A | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+9593G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298717 | ||||||
| chr1:44298778
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.758+9532G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298778 | ||||||
| chr1:44298875
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.758+9435A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298875 | ||||||
| chr1:44298946
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.758+9364G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298946 | ||||||
| chr1:44299005
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+9305G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299005 | ||||||
| chr1:44299180
|
T | C | 2 | a0001c0001t0001g0297a0001c0001t0001g0299 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.758+9130A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299180 | ||||||
| chr1:44299239
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.758+9071C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299239 | ||||||
| chr1:44299349
|
TTTTTTA | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0334a0001c0001t0001g0335others(2): Show | 5 | HG01261.hp2 HG02293.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+8955_758+8960d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299349 | ||||||
| chr1:44299398
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.758+8912T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299398 | ||||||
| chr1:44299942
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.758+8368G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299942 | ||||||
| chr1:44299974
|
C | T | 9 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0237others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.758+8336G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299974 | ||||||
| chr1:44300182
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.758+8128C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300182 | ||||||
| chr1:44300208
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.758+8102C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300208 | ||||||
| chr1:44300359
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.758+7951C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300359 | ||||||
| chr1:44300399
|
C | T | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+7911G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300399 | ||||||
| chr1:44300419
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.758+7891C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300419 | ||||||
| chr1:44300496
|
G | C | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.758+7814C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300496 | ||||||
| chr1:44300637
|
T | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0147a0001c0001t0001g0150others(3): Show | 6 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+7673A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300637 | ||||||
| chr1:44300659
|
T | A | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+7651A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300659 | ||||||
| chr1:44300725
|
C | T | 27 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(24): Show | 27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.758+7585G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300725 | ||||||
| chr1:44300943
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.758+7367C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300943 | ||||||
| chr1:44301024
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.758+7286C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301024 | ||||||
| chr1:44301042
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+7268A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301042 | ||||||
| chr1:44301263
|
C | T | 95 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(92): Show | 95 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.758+7047G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301263 | ||||||
| chr1:44301299
|
C | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.758+7011G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301299 | ||||||
| chr1:44301417
|
A | C | 1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.758+6893T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301417 | ||||||
| chr1:44301506
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.758+6804G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301506 | ||||||
| chr1:44301507
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+6803A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301507 | ||||||
| chr1:44301693
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+6617C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301693 | ||||||
| chr1:44301760
|
T | C | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.758+6550A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301760 | ||||||
| chr1:44301776
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.758+6534A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301776 | ||||||
| chr1:44301802
|
C | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0272others(4): Show | 7 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.758+6508G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301802 | ||||||
| chr1:44301868
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.758+6442G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301868 | ||||||
| chr1:44302023
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+6287A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302023 | ||||||
| chr1:44302078
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+6232T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302078 | ||||||
| chr1:44302180
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.758+6130C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302180 | ||||||
| chr1:44302241
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.758+6069A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302241 | ||||||
| chr1:44302312
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.758+5998T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302312 | ||||||
| chr1:44302341
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.758+5969C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302341 | ||||||
| chr1:44302467
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.758+5843C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302467 | ||||||
| chr1:44302577
|
T | G | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+5733A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302577 | ||||||
| chr1:44302637
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.758+5673A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302637 | ||||||
| chr1:44302720
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+5590A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302720 | ||||||
| chr1:44302725
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.758+5585G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302725 | ||||||
| chr1:44302771
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+5539G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302771 | ||||||
| chr1:44302965
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.758+5345T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302965 | ||||||
| chr1:44303273
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.758+5037A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303273 | ||||||
| chr1:44303451
|
G | T | 7 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0257others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.758+4859C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303451 | ||||||
| chr1:44303550
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.758+4760A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303550 | ||||||
| chr1:44303691
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.758+4619T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303691 | ||||||
| chr1:44303743
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+4567T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303743 | ||||||
| chr1:44303935
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.758+4375A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303935 | ||||||
| chr1:44304140
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.758+4170C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304140 | ||||||
| chr1:44304147
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.758+4163A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304147 | ||||||
| chr1:44304302
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.758+4008A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304302 | ||||||
| chr1:44304357
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.758+3953G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304357 | ||||||
| chr1:44304357
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.758+3953G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304357 | ||||||
| chr1:44304545
|
C | T | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+3765G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304545 | ||||||
| chr1:44304598
|
A | AC | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+3711dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304598 | ||||||
| chr1:44304807
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.758+3503T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304807 | ||||||
| chr1:44304859
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | NA18959.hp1 NA18970.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+3451C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304859 | ||||||
| chr1:44304900
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.758+3410A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304900 | ||||||
| chr1:44305419
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.758+2891C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305419 | ||||||
| chr1:44305708
|
TATC | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+2599_758+2601d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305708 | ||||||
| chr1:44305802
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+2508C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305802 | ||||||
| chr1:44305813
|
T | C | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.758+2497A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305813 | ||||||
| chr1:44305982
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.758+2328G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305982 | ||||||
| chr1:44306163
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.758+2147G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306163 | ||||||
| chr1:44306226
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758+2084A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306226 | ||||||
| chr1:44306409
|
C | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.758+1901G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306409 | ||||||
| chr1:44306421
|
G | A | 18 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0135others(15): Show | 18 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.758+1889C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306421 | ||||||
| chr1:44306421
|
G | C | 1 | a0001c0001t0001g0013 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.758+1889C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306421 | ||||||
| chr1:44306428
|
G | A | 3 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG01167.hp2 HG01169.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.758+1882C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306428 | ||||||
| chr1:44306662
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+1648G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306662 | ||||||
| chr1:44306697
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.758+1613G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306697 | ||||||
| chr1:44306730
|
C | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.758+1580G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306730 | ||||||
| chr1:44306867
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.758+1443C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306867 | ||||||
| chr1:44306954
|
T | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.758+1356A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306954 | ||||||
| chr1:44307059
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+1251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307059 | ||||||
| chr1:44307087
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+1223A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307087 | ||||||
| chr1:44307211
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.758+1099A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307211 | ||||||
| chr1:44307384
|
C | A | 2 | a0001c0001t0001g0302a0001c0004t0001g0258 | 2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.758+926G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307384 | ||||||
| chr1:44307543
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.758+767G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307543 | ||||||
| chr1:44307554
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.758+756C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307554 | ||||||
| chr1:44307696
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.758+614C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307696 | ||||||
| chr1:44307853
|
C | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.758+457G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307853 | ||||||
| chr1:44307963
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.758+347A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307963 | ||||||
| chr1:44308055
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.758+255C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44308055 | ||||||
| chr1:44308167
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.758+143G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44308167 | ||||||
| chr1:44308511
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.667-110A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308511 | ||||||
| chr1:44308615
|
T | C | 28 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.667-214A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308615 | ||||||
| chr1:44308624
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.667-223C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308624 | ||||||
| chr1:44308667
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-266T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308667 | ||||||
| chr1:44308955
|
G | A | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.667-554C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308955 | ||||||
| chr1:44309340
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.667-939G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309340 | ||||||
| chr1:44309701
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.667-1300T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309701 | ||||||
| chr1:44309810
|
G | A | 3 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG01167.hp2 HG01169.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.667-1409C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309810 | ||||||
| chr1:44309881
|
G | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.667-1480C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309881 | ||||||
| chr1:44309936
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.667-1535G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309936 | ||||||
| chr1:44309984
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-1583C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309984 | ||||||
| chr1:44309989
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1588C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309989 | ||||||
| chr1:44310043
|
T | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.667-1642A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310043 | ||||||
| chr1:44310155
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.667-1754G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310155 | ||||||
| chr1:44310192
|
AG | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.667-1792delC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310192 | ||||||
| chr1:44310323
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.667-1922G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310323 | ||||||
| chr1:44310379
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.667-1978G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310379 | ||||||
| chr1:44310460
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.667-2059T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310460 | ||||||
| chr1:44310510
|
T | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.667-2109A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310510 | ||||||
| chr1:44310535
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-2134C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310535 | ||||||
| chr1:44310536
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.667-2135C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310536 | ||||||
| chr1:44310568
|
C | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.667-2167G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310568 | ||||||
| chr1:44310688
|
G | T | 100 | a0001c0001t0001g0110a0001c0001t0001g0221a0001c0001t0001g0227others(97): Show | 100 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.667-2287C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310688 | ||||||
| chr1:44310771
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.667-2370T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310771 | ||||||
| chr1:44310910
|
GTCTCTCT others(24): Show |
G | 1 | a0001c0001t0001g0329 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.666+2228_666+2258d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310910 | ||||||
| chr1:44310943
|
T | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0186others(1): Show | 4 | HG02895.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+2226A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310943 | ||||||
| chr1:44310946
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.666+2223C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310946 | ||||||
| chr1:44310951
|
T | TCG | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0016others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.666+2216_666+2217d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCG | 18 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0032others(15): Show | 18 | HG00673.hp1 HG02056.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.666+2214_666+2217d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCG | 6 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0039others(3): Show | 6 | HG00733.hp2 HG03130.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+2212_666+2217d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(1): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(4): Show | 7 | HG00408.hp1 HG00738.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+2210_666+2217d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(3): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0042 | 2 | NA18951.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.666+2208_666+2217d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(5): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0082 | 2 | HG01109.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.666+2206_666+2217d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(7): Show |
1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.666+2217_666+2218i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(10): Show |
1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.666+2217_666+2218i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGCGCGC others(6): Show |
1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.666+2217_666+2218i others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310951
|
T | TCGTGCGC others(5): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0203 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.666+2217_666+2218i others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | ||||||
| chr1:44310952
|
C | A | 18 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(15): Show | 18 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.666+2217G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310952 | ||||||
| chr1:44310954
|
C | CGCGCGCG others(10): Show |
1 | a0001c0001t0001g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.666+2214_666+2215i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310954 | ||||||
| chr1:44310954
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.666+2215G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310954 | ||||||
| chr1:44310957
|
G | GCGCTGCG others(10): Show |
1 | a0001c0001t0001g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.666+2211_666+2212i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310957 | ||||||
| chr1:44310958
|
C | CA | 9 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0139others(6): Show | 9 | HG02818.hp2 NA18959.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+2210_666+2211i others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310958 | ||||||
| chr1:44310959
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2210C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310959 | ||||||
| chr1:44310959
|
GCGCGCAC others(11): Show |
G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | NA18941.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.666+2192_666+2209d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310959 | ||||||
| chr1:44310960
|
C | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0159 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.666+2209G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310960 | ||||||
| chr1:44310961
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.666+2208C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310961 | ||||||
| chr1:44310962
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.666+2207G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310962 | ||||||
| chr1:44310962
|
C | CGCGCGCG others(4): Show |
1 | a0001c0001t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+2206_666+2207i others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310962 | ||||||
| chr1:44310963
|
G | GCGCGCGC others(13): Show |
1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.666+2205_666+2206i others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCA | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(49): Show | 52 | HG00558.hp1 HG00673.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.666+2204_666+2205d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACA | G | 42 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0065others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.666+2202_666+2205d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACA | G | 25 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0062others(22): Show | 25 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.666+2200_666+2205d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(1): Show |
G | 20 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0001g0142others(17): Show | 20 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.666+2198_666+2205d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(3): Show |
G | 8 | a0001c0001t0001g0050a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG00280.hp2 HG01167.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.666+2196_666+2205d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(5): Show |
G | 6 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0122others(3): Show | 6 | HG02717.hp1 HG02965.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+2194_666+2205d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(7): Show |
G | 7 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0106others(4): Show | 7 | HG02148.hp1 NA18939.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+2192_666+2205d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(9): Show |
G | 11 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0100others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+2190_666+2205d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310963
|
GCACACAC others(11): Show |
G | 11 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0240others(8): Show | 11 | HG00733.hp1 HG01175.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+2188_666+2205d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | ||||||
| chr1:44310964
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.666+2205G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310964 | ||||||
| chr1:44310965
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.666+2204T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310965 | ||||||
| chr1:44310967
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 190 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.666+2202T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310967 | ||||||
| chr1:44310967
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2202T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310967 | ||||||
| chr1:44310968
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2201G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310968 | ||||||
| chr1:44310969
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 224 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.666+2200T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310969 | ||||||
| chr1:44310971
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.666+2198T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310971 | ||||||
| chr1:44310973
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 156 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.666+2196T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310973 | ||||||
| chr1:44310974
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666+2195G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310974 | ||||||
| chr1:44310975
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.666+2194T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310975 | ||||||
| chr1:44310977
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.666+2192T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310977 | ||||||
| chr1:44310979
|
A | G | 24 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0001g0063others(21): Show | 24 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.666+2190T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310979 | ||||||
| chr1:44310981
|
A | G | 18 | a0001c0001t0001g0050a0001c0001t0001g0063a0001c0001t0001g0094others(15): Show | 18 | HG00438.hp1 HG01261.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.666+2188T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310981 | ||||||
| chr1:44310983
|
A | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0105a0001c0001t0001g0108others(4): Show | 7 | HG02818.hp1 HG03209.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+2186T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310983 | ||||||
| chr1:44310985
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0108 | 2 | HG02818.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.666+2184T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310985 | ||||||
| chr1:44310986
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2183G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310986 | ||||||
| chr1:44310987
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0164 | 2 | NA19030.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.666+2182T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310987 | ||||||
| chr1:44310989
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2180T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310989 | ||||||
| chr1:44310991
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2178T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310991 | ||||||
| chr1:44311015
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666+2154T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311015 | ||||||
| chr1:44311016
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666+2153G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311016 | ||||||
| chr1:44311017
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.666+2152C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311017 | ||||||
| chr1:44311029
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.666+2140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311029 | ||||||
| chr1:44311512
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.666+1657G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311512 | ||||||
| chr1:44311918
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.666+1251A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311918 | ||||||
| chr1:44312157
|
C | G | 1 | a0001c0001t0001g0007 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.666+1012G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312157 | ||||||
| chr1:44312300
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.666+869C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312300 | ||||||
| chr1:44312394
|
T | C | 1 | a0001c0004t0001g0258 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.666+775A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312394 | ||||||
| chr1:44312738
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.666+431G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312738 | ||||||
| chr1:44312819
|
T | C | 5 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0001t0001g0187others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+350A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312819 | ||||||
| chr1:44312908
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.666+261A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312908 | ||||||
| chr1:44312980
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+189G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312980 | ||||||
| chr1:44313295
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.607-67G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313295 | ||||||
| chr1:44313475
|
G | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-247C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313475 | ||||||
| chr1:44313528
|
A | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(3): Show | 6 | HG02723.hp2 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-300T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313528 | ||||||
| chr1:44313657
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02717.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.607-429A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313657 | ||||||
| chr1:44313814
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0152 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.607-586G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313814 | ||||||
| chr1:44313892
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0138others(3): Show | 6 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-664A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313892 | ||||||
| chr1:44313985
|
T | TA | 9 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-758dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313985 | ||||||
| chr1:44314075
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.607-847G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314075 | ||||||
| chr1:44314139
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG02056.hp2 HG02132.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.607-911A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314139 | ||||||
| chr1:44314153
|
T | TG | 176 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0044others(173): Show | 176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.607-926dupC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314153 | ||||||
| chr1:44314248
|
G | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0057others(3): Show | 6 | HG02040.hp1 HG02080.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-1020C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314248 | ||||||
| chr1:44314319
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.607-1091G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314319 | ||||||
| chr1:44314339
|
G | T | 1 | a0001c0001t0001g0337 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.607-1111C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314339 | ||||||
| chr1:44314526
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-1298A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314526 | ||||||
| chr1:44314559
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.607-1331C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314559 | ||||||
| chr1:44314650
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.607-1422G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314650 | ||||||
| chr1:44314740
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-1512C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314740 | ||||||
| chr1:44314779
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.607-1551G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314779 | ||||||
| chr1:44314896
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.607-1668G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314896 | ||||||
| chr1:44314901
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.607-1673A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314901 | ||||||
| chr1:44314947
|
A | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-1719T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314947 | ||||||
| chr1:44315123
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.607-1895T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315123 | ||||||
| chr1:44315371
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-2143T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315371 | ||||||
| chr1:44315480
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2252G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315480 | ||||||
| chr1:44315611
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607-2383A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315611 | ||||||
| chr1:44315664
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.607-2436A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315664 | ||||||
| chr1:44315811
|
C | A | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.607-2583G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315811 | ||||||
| chr1:44315983
|
CT | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.607-2756delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315983 | ||||||
| chr1:44316087
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2859A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316087 | ||||||
| chr1:44316306
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.607-3078C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316306 | ||||||
| chr1:44316919
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.606+2709G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316919 | ||||||
| chr1:44317000
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.606+2628A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317000 | ||||||
| chr1:44317082
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2546A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317082 | ||||||
| chr1:44317117
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+2511C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317117 | ||||||
| chr1:44317144
|
G | GCA | 116 | a0001c0001t0001g0117a0001c0001t0001g0126a0001c0001t0001g0132others(113): Show | 116 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.606+2482_606+2483d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
G | GCACA | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 103 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.606+2480_606+2483d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
G | GCACACA | 16 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0038others(13): Show | 16 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+2478_606+2483d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
G | GCACACAC others(1): Show |
18 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(15): Show | 18 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.606+2476_606+2483d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0059others(4): Show | 7 | HG01106.hp2 HG01256.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+2474_606+2483d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.606+2472_606+2483d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317144
|
GCA | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0205a0001c0001t0001g0326 | 3 | HG02040.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.606+2482_606+2483d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | ||||||
| chr1:44317499
|
G | GACAGAAA others(22): Show |
4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2100_606+2128d others(31): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317499 | ||||||
| chr1:44317585
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0297others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2043C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317585 | ||||||
| chr1:44317649
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.606+1979A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317649 | ||||||
| chr1:44317695
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.606+1933G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317695 | ||||||
| chr1:44317813
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.606+1815T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317813 | ||||||
| chr1:44318058
|
G | A | 1 | a0001c0001t0001g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.606+1570C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318058 | ||||||
| chr1:44318300
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.606+1328C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318300 | ||||||
| chr1:44318603
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.606+1025C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318603 | ||||||
| chr1:44318620
|
C | T | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.606+1008G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318620 | ||||||
| chr1:44318699
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+929T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318699 | ||||||
| chr1:44318725
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.606+903G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318725 | ||||||
| chr1:44318812
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.606+816T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318812 | ||||||
| chr1:44319045
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.606+583A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319045 | ||||||
| chr1:44319110
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.606+518G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319110 | ||||||
| chr1:44319174
|
T | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+454A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319174 | ||||||
| chr1:44319199
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.606+429C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319199 | ||||||
| chr1:44319321
|
A | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.606+307T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319321 | ||||||
| chr1:44319325
|
C | T | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.606+303G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319325 | ||||||
| chr1:44319899
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-155C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44319899 | ||||||
| chr1:44320014
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.490-270G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320014 | ||||||
| chr1:44320159
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-415T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320159 | ||||||
| chr1:44320400
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.490-656T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320400 | ||||||
| chr1:44320502
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.490-758G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320502 | ||||||
| chr1:44320519
|
G | A | 1 | a0001c0002t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490-775C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320519 | ||||||
| chr1:44320564
|
G | A | 5 | a0001c0001t0001g0241a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG00544.hp2 NA18963.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-820C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320564 | ||||||
| chr1:44320711
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.490-967G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320711 | ||||||
| chr1:44321061
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.490-1317T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321061 | ||||||
| chr1:44321503
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.490-1759A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321503 | ||||||
| chr1:44321566
|
C | A | 7 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0257others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1822G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321566 | ||||||
| chr1:44321608
|
A | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0268a0001c0001t0001g0289others(2): Show | 5 | HG00738.hp1 HG01256.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-1864T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321608 | ||||||
| chr1:44321660
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0091 | 2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.490-1916G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321660 | ||||||
| chr1:44321994
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.490-2250T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321994 | ||||||
| chr1:44322101
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2357G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322101 | ||||||
| chr1:44322306
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490-2562C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322306 | ||||||
| chr1:44322726
|
A | T | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.490-2982T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322726 | ||||||
| chr1:44323243
|
T | C | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-3499A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323243 | ||||||
| chr1:44323558
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0288a0001c0001t0001g0311 | 3 | NA18952.hp2 NA19004.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.490-3814G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323558 | ||||||
| chr1:44323583
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-3839A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323583 | ||||||
| chr1:44323593
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-3849C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323593 | ||||||
| chr1:44324050
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.490-4306C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324050 | ||||||
| chr1:44324221
|
A | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4477T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324221 | ||||||
| chr1:44324394
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-4650A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324394 | ||||||
| chr1:44324433
|
CTGTT | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4693_490-4690d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324433 | ||||||
| chr1:44324455
|
G | C | 27 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(24): Show | 27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-4711C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324455 | ||||||
| chr1:44324476
|
C | CT | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 184 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.490-4733dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324476 | ||||||
| chr1:44324476
|
C | CTT | 19 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(16): Show | 19 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4734_490-4733d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324476 | ||||||
| chr1:44324630
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4886G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324630 | ||||||
| chr1:44324718
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.490-4974C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324718 | ||||||
| chr1:44324851
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-5107T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324851 | ||||||
| chr1:44324870
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG02056.hp2 HG02132.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.490-5126G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324870 | ||||||
| chr1:44324894
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-5150T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324894 | ||||||
| chr1:44324981
|
T | C | 106 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(103): Show | 106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.490-5237A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324981 | ||||||
| chr1:44325057
|
C | A | 1 | a0001c0001t0001g0334 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.490-5313G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325057 | ||||||
| chr1:44325075
|
CT | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.490-5332delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325075 | ||||||
| chr1:44325075
|
CTT | C | 101 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0228others(98): Show | 101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.490-5333_490-5332d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325075 | ||||||
| chr1:44325156
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.490-5412A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325156 | ||||||
| chr1:44325163
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5419G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325163 | ||||||
| chr1:44325327
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.490-5583C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325327 | ||||||
| chr1:44325354
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-5610G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325354 | ||||||
| chr1:44325522
|
T | C | 24 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0147others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-5778A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325522 | ||||||
| chr1:44325561
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5817T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325561 | ||||||
| chr1:44325850
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-6106G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325850 | ||||||
| chr1:44326175
|
G | A | 7 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0303others(4): Show | 7 | NA18966.hp2 NA19012.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-6431C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326175 | ||||||
| chr1:44326274
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-6530T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326274 | ||||||
| chr1:44326345
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-6601A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326345 | ||||||
| chr1:44326464
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.490-6720G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326464 | ||||||
| chr1:44326653
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.490-6909A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326653 | ||||||
| chr1:44326841
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.490-7097G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326841 | ||||||
| chr1:44326996
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.490-7252G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326996 | ||||||
| chr1:44327009
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.490-7265A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327009 | ||||||
| chr1:44327666
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.490-7922G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327666 | ||||||
| chr1:44327746
|
T | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8002A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327746 | ||||||
| chr1:44327779
|
A | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8035T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327779 | ||||||
| chr1:44327981
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.490-8237G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327981 | ||||||
| chr1:44327985
|
G | C | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-8241C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327985 | ||||||
| chr1:44327995
|
A | G | 73 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0116others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.490-8251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327995 | ||||||
| chr1:44328088
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 96 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-8344C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328088 | ||||||
| chr1:44328234
|
C | T | 4 | a0001c0001t0001g0229a0001c0001t0001g0238a0001c0001t0001g0300others(1): Show | 4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8490G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328234 | ||||||
| chr1:44328248
|
C | G | 7 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0303others(4): Show | 7 | NA18966.hp2 NA19012.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-8504G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328248 | ||||||
| chr1:44328409
|
T | A | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.490-8665A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328409 | ||||||
| chr1:44329134
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-9390G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329134 | ||||||
| chr1:44329253
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-9509G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329253 | ||||||
| chr1:44329600
|
A | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0267 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.489+9445T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329600 | ||||||
| chr1:44329789
|
G | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+9256C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329789 | ||||||
| chr1:44330124
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.489+8921G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44330124 | ||||||
| chr1:44331130
|
C | G | 29 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(26): Show | 29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+7915G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331130 | ||||||
| chr1:44331262
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+7783A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331262 | ||||||
| chr1:44331270
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.489+7775T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331270 | ||||||
| chr1:44331301
|
AT | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0076others(6): Show | 9 | HG01169.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+7743delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331301 | ||||||
| chr1:44331328
|
A | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+7717T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331328 | ||||||
| chr1:44331474
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+7571A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331474 | ||||||
| chr1:44331573
|
C | G | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.489+7472G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331573 | ||||||
| chr1:44331719
|
A | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+7326T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331719 | ||||||
| chr1:44331794
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.489+7251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331794 | ||||||
| chr1:44331808
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+7237A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331808 | ||||||
| chr1:44331836
|
G | T | 10 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0234others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+7209C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331836 | ||||||
| chr1:44331867
|
T | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0183 | 2 | HG00423.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.489+7178A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331867 | ||||||
| chr1:44332258
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+6787A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332258 | ||||||
| chr1:44332332
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+6713G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332332 | ||||||
| chr1:44332372
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0238a0001c0001t0001g0300others(1): Show | 4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6673C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332372 | ||||||
| chr1:44332451
|
C | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(3): Show | 6 | NA18939.hp1 NA18941.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+6594G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332451 | ||||||
| chr1:44332519
|
A | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0057others(2): Show | 5 | HG02080.hp2 NA18954.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+6526T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332519 | ||||||
| chr1:44332669
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0164others(1): Show | 4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6376G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332669 | ||||||
| chr1:44332700
|
G | A | 72 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.489+6345C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332700 | ||||||
| chr1:44332703
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6342T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332703 | ||||||
| chr1:44332863
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+6182A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332863 | ||||||
| chr1:44332867
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+6178C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332867 | ||||||
| chr1:44332978
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.489+6067C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332978 | ||||||
| chr1:44333067
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.489+5978A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333067 | ||||||
| chr1:44333110
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.489+5935A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333110 | ||||||
| chr1:44333113
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+5932A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333113 | ||||||
| chr1:44333319
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | HG02258.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.489+5726C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333319 | ||||||
| chr1:44333325
|
G | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+5720C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333325 | ||||||
| chr1:44333362
|
C | A | 28 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.489+5683G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333362 | ||||||
| chr1:44333406
|
C | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5639G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333406 | ||||||
| chr1:44333452
|
A | G | 1 | a0001c0001t0001g0323 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.489+5593T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333452 | ||||||
| chr1:44333505
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.489+5540G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333505 | ||||||
| chr1:44333630
|
C | T | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+5415G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333630 | ||||||
| chr1:44333711
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.489+5334G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333711 | ||||||
| chr1:44333872
|
C | T | 11 | a0001c0001t0001g0110a0001c0001t0001g0231a0001c0001t0001g0232others(8): Show | 11 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+5173G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333872 | ||||||
| chr1:44333927
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+5118C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333927 | ||||||
| chr1:44334018
|
G | T | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5027C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334018 | ||||||
| chr1:44334023
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.489+5022G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334023 | ||||||
| chr1:44334129
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489+4916G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334129 | ||||||
| chr1:44334280
|
T | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0085others(1): Show | 4 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+4765A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334280 | ||||||
| chr1:44334333
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.489+4712T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334333 | ||||||
| chr1:44334588
|
A | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+4457T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334588 | ||||||
| chr1:44334708
|
C | G | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+4337G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334708 | ||||||
| chr1:44334826
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0036others(16): Show | 19 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+4219C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334826 | ||||||
| chr1:44334868
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+4177A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334868 | ||||||
| chr1:44334878
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+4167T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334878 | ||||||
| chr1:44335116
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.489+3929A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335116 | ||||||
| chr1:44335168
|
C | T | 3 | a0001c0001t0002g0230a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.489+3877G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335168 | ||||||
| chr1:44335219
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.489+3826G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335219 | ||||||
| chr1:44335313
|
A | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+3732T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335313 | ||||||
| chr1:44335320
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3725T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335320 | ||||||
| chr1:44335354
|
C | CA | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+3690dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335354 | ||||||
| chr1:44335425
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+3620T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335425 | ||||||
| chr1:44335489
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+3556C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335489 | ||||||
| chr1:44335499
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.489+3546G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335499 | ||||||
| chr1:44335502
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.489+3543C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335502 | ||||||
| chr1:44335547
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+3498C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335547 | ||||||
| chr1:44335576
|
A | G | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.489+3469T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335576 | ||||||
| chr1:44335588
|
G | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(335): Show | 338 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.489+3457C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335588 | ||||||
| chr1:44335699
|
C | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3346G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335699 | ||||||
| chr1:44335776
|
C | CA | 15 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0136others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+3268dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335776 | ||||||
| chr1:44335992
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.489+3053A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335992 | ||||||
| chr1:44336017
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.489+3028A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336017 | ||||||
| chr1:44336396
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2649C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336396 | ||||||
| chr1:44336553
|
TA | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.489+2491delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336553 | ||||||
| chr1:44336977
|
T | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.489+2068A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336977 | ||||||
| chr1:44337565
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+1480G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337565 | ||||||
| chr1:44337674
|
T | C | 99 | a0001c0001t0001g0110a0001c0001t0001g0227a0001c0001t0001g0228others(96): Show | 99 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.489+1371A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337674 | ||||||
| chr1:44337799
|
T | A | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.489+1246A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337799 | ||||||
| chr1:44337831
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+1214C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337831 | ||||||
| chr1:44337840
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+1205C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337840 | ||||||
| chr1:44337843
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.489+1202C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337843 | ||||||
| chr1:44338241
|
T | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+804A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338241 | ||||||
| chr1:44338344
|
C | T | 18 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0166others(15): Show | 18 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+701G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338344 | ||||||
| chr1:44338457
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0311 | 2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.489+588A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338457 | ||||||
| chr1:44338489
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.489+556T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338489 | ||||||
| chr1:44338586
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+459C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338586 | ||||||
| chr1:44338686
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.489+359T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338686 | ||||||
| chr1:44338808
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+237C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338808 | ||||||
| chr1:44338961
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+84G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338961 | ||||||
| chr1:44339340
|
TA | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0073others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.212-19delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339340 | ||||||
| chr1:44339341
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.212-19T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339341 | ||||||
| chr1:44339354
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.212-32T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339354 | ||||||
| chr1:44339689
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-367G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339689 | ||||||
| chr1:44340023
|
T | G | 1 | a0001c0001t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-701A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340023 | ||||||
| chr1:44340034
|
TCGA | T | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-715_212-713del others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340034 | ||||||
| chr1:44340145
|
T | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0155others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-823A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340145 | ||||||
| chr1:44340149
|
CA | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.212-828delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340149 | ||||||
| chr1:44341064
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-1742G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341064 | ||||||
| chr1:44341466
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.212-2144A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341466 | ||||||
| chr1:44341492
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.212-2170G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341492 | ||||||
| chr1:44341497
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-2175C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341497 | ||||||
| chr1:44341542
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 231 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.212-2220A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341542 | ||||||
| chr1:44341718
|
C | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | NA18970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.212-2396G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341718 | ||||||
| chr1:44341890
|
AAAAAC | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-2573_212-2569d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341890 | ||||||
| chr1:44341938
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-2616C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341938 | ||||||
| chr1:44341990
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-2668C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341990 | ||||||
| chr1:44342113
|
C | A | 15 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-2791G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342113 | ||||||
| chr1:44342121
|
T | C | 70 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.212-2799A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342121 | ||||||
| chr1:44342515
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3193C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342515 | ||||||
| chr1:44342519
|
C | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3197G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342519 | ||||||
| chr1:44342535
|
T | TAC | 29 | a0001c0001t0001g0031a0001c0001t0001g0121a0001c0001t0001g0124others(26): Show | 29 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.212-3215_212-3214d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342535 | ||||||
| chr1:44342643
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.212-3321A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342643 | ||||||
| chr1:44342646
|
C | T | 29 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(26): Show | 29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-3324G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342646 | ||||||
| chr1:44342653
|
G | GT | 15 | a0001c0001t0001g0228a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-3332dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342653 | ||||||
| chr1:44342789
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.212-3467C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342789 | ||||||
| chr1:44342811
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 230 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.212-3489A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342811 | ||||||
| chr1:44342812
|
A | AATAT | 3 | a0001c0001t0001g0022a0001c0001t0001g0284a0001c0001t0001g0300 | 3 | HG01361.hp1 NA18939.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.212-3494_212-3491d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.212-3500_212-3491d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-3504_212-3491d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.212-3506_212-3491d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.212-3490T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0269a0001c0001t0001g0308 | 2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-3502_212-3491d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342812
|
AATATATA others(19): Show |
A | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.212-3516_212-3491d others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | ||||||
| chr1:44342813
|
A | C | 1 | a0001c0001t0001g0035 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.212-3491T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342813 | ||||||
| chr1:44342814
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-3492A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342814 | ||||||
| chr1:44342820
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0133a0001c0003t0001g0214 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.212-3499_212-3498i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342820 | ||||||
| chr1:44342820
|
T | TATATATA others(32): Show |
1 | a0001c0001t0001g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.212-3499_212-3498i others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342820 | ||||||
| chr1:44342821
|
ATATATAT others(33): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.212-3539_212-3500d others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342821 | ||||||
| chr1:44342822
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.212-3501_212-3500i others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342822 | ||||||
| chr1:44342824
|
T | TATATATA others(3): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0222 | 2 | HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.212-3503_212-3502i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342824 | ||||||
| chr1:44342824
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.212-3503_212-3502i others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342824 | ||||||
| chr1:44342826
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.212-3505_212-3504i others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342826 | ||||||
| chr1:44342827
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.212-3536_212-3506d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342827 | ||||||
| chr1:44342827
|
ATATATAT others(25): Show |
A | 16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 16 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-3537_212-3506d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342827 | ||||||
| chr1:44342828
|
T | TATATAA | 13 | a0001c0001t0001g0130a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01106.hp1 HG01361.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-3507_212-3506i others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342828 | ||||||
| chr1:44342828
|
T | TATATAAA others(33): Show |
1 | a0001c0001t0001g0184 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.212-3507_212-3506i others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342828 | ||||||
| chr1:44342829
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.212-3537_212-3508d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | ||||||
| chr1:44342829
|
ATATATAT others(25): Show |
A | 2 | a0001c0001t0001g0114a0001c0001t0001g0119 | 2 | HG02293.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.212-3539_212-3508d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | ||||||
| chr1:44342829
|
ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0015 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.212-3545_212-3508d others(40): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | ||||||
| chr1:44342830
|
TATATATA others(20): Show |
T | 1 | a0001c0001t0001g0334 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.212-3535_212-3509d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342830 | ||||||
| chr1:44342831
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.212-3546_212-3510d others(39): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342831 | ||||||
| chr1:44342833
|
ATATATAT others(21): Show |
A | 3 | a0001c0001t0002g0230a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.212-3539_212-3512d others(30): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342833 | ||||||
| chr1:44342834
|
T | A | 28 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(25): Show | 28 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.212-3512A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342834 | ||||||
| chr1:44342835
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-3540_212-3514d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342835 | ||||||
| chr1:44342835
|
ATATATAT others(28): Show |
A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.212-3548_212-3514d others(37): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342835 | ||||||
| chr1:44342836
|
T | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG02922.hp2 NA18949.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-3514A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342836 | ||||||
| chr1:44342836
|
TATATATA others(14): Show |
T | 2 | a0001c0001t0001g0116a0001c0001t0001g0335 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.212-3535_212-3515d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342836 | ||||||
| chr1:44342837
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0123a0001c0001t0001g0255 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.212-3538_212-3516d others(25): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | ||||||
| chr1:44342837
|
ATATATAT others(23): Show |
A | 4 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3545_212-3516d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | ||||||
| chr1:44342837
|
ATATATAT others(28): Show |
A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG01243.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.212-3550_212-3516d others(37): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | ||||||
| chr1:44342838
|
T | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-3516A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342838 | ||||||
| chr1:44342839
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.212-3538_212-3518d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | ||||||
| chr1:44342839
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.212-3539_212-3518d others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | ||||||
| chr1:44342839
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.212-3544_212-3518d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | ||||||
| chr1:44342839
|
ATATATAT others(23): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0208 | 2 | HG02056.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-3547_212-3518d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | ||||||
| chr1:44342841
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212-3545_212-3520d others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | ||||||
| chr1:44342841
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.212-3548_212-3520d others(31): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | ||||||
| chr1:44342841
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-3551_212-3520d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | ||||||
| chr1:44342843
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.212-3542_212-3522d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342843 | ||||||
| chr1:44342844
|
T | A | 1 | a0001c0001t0005g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212-3522A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342844 | ||||||
| chr1:44342845
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0027 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.212-3539_212-3524d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342845 | ||||||
| chr1:44342845
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.212-3547_212-3524d others(26): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342845 | ||||||
| chr1:44342847
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.212-3538_212-3526d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342847 | ||||||
| chr1:44342847
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0162a0001c0001t0001g0297 | 2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.212-3542_212-3526d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342847 | ||||||
| chr1:44342848
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.212-3526A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342848 | ||||||
| chr1:44342849
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0242a0001c0001t0001g0267 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.212-3537_212-3528d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342849
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.212-3540_212-3528d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342849
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.212-3541_212-3528d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342849
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212-3544_212-3528d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342849
|
ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0014a0001c0001t0001g0043 | 2 | NA18995.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.212-3545_212-3528d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342849
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0017 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.212-3546_212-3528d others(21): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | ||||||
| chr1:44342850
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212-3528A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342850 | ||||||
| chr1:44342851
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0280a0001c0001t0001g0314 | 2 | HG00438.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.212-3539_212-3530d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342851
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.212-3540_212-3530d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342851
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.212-3542_212-3530d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342851
|
ATATATAT others(7): Show |
A | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3543_212-3530d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342851
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.212-3544_212-3530d others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342851
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.212-3546_212-3530d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | ||||||
| chr1:44342853
|
ATATATTT others(3): Show |
A | 7 | a0001c0001t0001g0243a0001c0001t0001g0250a0001c0001t0001g0266others(4): Show | 7 | HG03017.hp2 HG04204.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-3541_212-3532d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0285 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.212-3542_212-3532d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.212-3543_212-3532d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(6): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.212-3544_212-3532d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(7): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.212-3545_212-3532d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(8): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.212-3546_212-3532d others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342853
|
ATATATTT others(10): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-3548_212-3532d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | ||||||
| chr1:44342855
|
ATATTTTT others(3): Show |
A | 3 | a0001c0001t0001g0093a0001c0001t0001g0170a0001c0001t0001g0321 | 3 | HG01884.hp1 NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.212-3543_212-3534d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | ||||||
| chr1:44342855
|
ATATTTTT others(4): Show |
A | 1 | a0001c0001t0001g0066 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.212-3544_212-3534d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | ||||||
| chr1:44342855
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0005 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.212-3545_212-3534d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | ||||||
| chr1:44342855
|
ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0325 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.212-3546_212-3534d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | ||||||
| chr1:44342857
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0139 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.212-3536_212-3535i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(70): Show |
1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(79): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0291 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-3536_212-3535i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
A | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0188a0001c0001t0001g0306others(3): Show | 6 | HG00733.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3535T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
AT | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0086others(5): Show | 8 | HG01257.hp1 HG01496.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-3536delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATT | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0199others(11): Show | 14 | HG00544.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-3537_212-3536d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTT | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0063others(3): Show | 6 | HG02630.hp1 HG03654.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3538_212-3536d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTT | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0026others(3): Show | 6 | HG01516.hp1 HG02080.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3539_212-3536d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTT | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0045others(7): Show | 10 | HG00642.hp1 HG00673.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-3540_212-3536d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTT | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(20): Show | 23 | HG00408.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-3541_212-3536d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT | A | 11 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0064others(8): Show | 11 | HG01516.hp2 HG02148.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-3542_212-3536d others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(1): Show |
A | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-3543_212-3536d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(2): Show |
A | 8 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0060others(5): Show | 8 | HG00544.hp1 HG00733.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-3544_212-3536d others(11): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(3): Show |
A | 11 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-3545_212-3536d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.212-3546_212-3536d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.212-3548_212-3536d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342857
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.212-3551_212-3536d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | ||||||
| chr1:44342858
|
T | TA | 4 | a0001c0001t0001g0115a0001c0001t0001g0157a0001c0001t0001g0198others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3537_212-3536i others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATA | 6 | a0001c0001t0001g0056a0001c0001t0001g0125a0001c0001t0001g0156others(3): Show | 6 | HG02738.hp2 HG02895.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3537_212-3536i others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATAAA others(30): Show |
4 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0138others(1): Show | 4 | HG00280.hp1 HG01433.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3537_212-3536i others(39): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0136 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(25): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(32): Show |
1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(34): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0142 | 2 | NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(43): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(58): Show |
1 | a0001c0001t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(67): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(62): Show |
1 | a0001c0001t0001g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(71): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(34): Show |
1 | a0001c0001t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(43): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(36): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0182 | 2 | NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(36): Show |
1 | a0001c0001t0001g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(38): Show |
1 | a0001c0001t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(47): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(40): Show |
1 | a0001c0001t0001g0137 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(49): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(42): Show |
1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(42): Show |
1 | a0001c0001t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(42): Show |
1 | a0001c0001t0001g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(12): Show |
1 | a0001c0001t0005g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(21): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342858
|
T | TATATATA others(18): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0155 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(27): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | ||||||
| chr1:44342859
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0035others(24): Show | 27 | HG00408.hp2 HG01106.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-3537A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342859 | ||||||
| chr1:44342860
|
T | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0056others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.212-3538A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342860 | ||||||
| chr1:44342861
|
T | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(21): Show | 24 | HG00544.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.212-3539A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342861 | ||||||
| chr1:44342862
|
T | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0044others(15): Show | 18 | HG01257.hp1 HG01496.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-3540A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342862 | ||||||
| chr1:44342863
|
T | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(18): Show | 21 | HG01175.hp1 HG01256.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.212-3541A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342863 | ||||||
| chr1:44342864
|
T | A | 22 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0032others(19): Show | 22 | HG00642.hp1 HG00673.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.212-3542A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342864 | ||||||
| chr1:44342865
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(24): Show | 27 | HG00408.hp1 HG01071.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-3543A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342865 | ||||||
| chr1:44342866
|
T | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0032others(20): Show | 23 | HG00642.hp1 HG00673.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-3544A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342866 | ||||||
| chr1:44342867
|
T | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00408.hp1 HG00639.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-3545A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342867 | ||||||
| chr1:44342868
|
T | A | 13 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0044others(10): Show | 13 | HG00544.hp1 HG00733.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-3546A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342868 | ||||||
| chr1:44342869
|
T | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00408.hp1 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-3547A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342869 | ||||||
| chr1:44342870
|
T | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG01496.hp2 NA18968.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3548A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342870 | ||||||
| chr1:44342871
|
T | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0199others(1): Show | 4 | HG01175.hp1 HG02040.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3549A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342871 | ||||||
| chr1:44342872
|
T | A | 1 | a0001c0001t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.212-3550A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342872 | ||||||
| chr1:44343115
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.212-3793A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343115 | ||||||
| chr1:44343236
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3914G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343236 | ||||||
| chr1:44343397
|
G | A | 22 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(19): Show | 22 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.212-4075C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343397 | ||||||
| chr1:44343556
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-4234G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343556 | ||||||
| chr1:44343766
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-4444A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343766 | ||||||
| chr1:44343773
|
T | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 261 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.212-4451A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343773 | ||||||
| chr1:44343986
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-4664G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343986 | ||||||
| chr1:44344045
|
C | T | 26 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0128others(23): Show | 26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.212-4723G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344045 | ||||||
| chr1:44344233
|
C | CAATA | 42 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0128others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.212-4915_212-4912d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344233
|
C | CAATAAAT others(1): Show |
8 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0001t0001g0184others(5): Show | 8 | HG01081.hp2 HG01257.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-4919_212-4912d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344233
|
CAATA | C | 99 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0052others(96): Show | 99 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.212-4915_212-4912d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344233
|
CAATAAAT others(1): Show |
C | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.212-4919_212-4912d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344233
|
CAATAAAT others(5): Show |
C | 6 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-4923_212-4912d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344233
|
CAATAAAT others(13): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.212-4931_212-4912d others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | ||||||
| chr1:44344276
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.212-4954A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344276 | ||||||
| chr1:44344506
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.212-5184C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344506 | ||||||
| chr1:44344740
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.212-5418G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344740 | ||||||
| chr1:44344932
|
G | C | 1 | a0001c0001t0001g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.212-5610C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344932 | ||||||
| chr1:44344946
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.212-5624G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344946 | ||||||
| chr1:44345001
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.212-5679T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345001 | ||||||
| chr1:44345383
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-6061G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345383 | ||||||
| chr1:44345741
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-6419G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345741 | ||||||
| chr1:44345902
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.212-6580G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345902 | ||||||
| chr1:44346138
|
C | T | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+6712G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346138 | ||||||
| chr1:44346173
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6677C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346173 | ||||||
| chr1:44346519
|
C | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+6331G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346519 | ||||||
| chr1:44346966
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+5884A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346966 | ||||||
| chr1:44347320
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.211+5530T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347320 | ||||||
| chr1:44347409
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.211+5441A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347409 | ||||||
| chr1:44347575
|
C | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+5275G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347575 | ||||||
| chr1:44347775
|
T | TA | 25 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(22): Show | 25 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.211+5074dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347775 | ||||||
| chr1:44347775
|
TA | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 232 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.211+5074delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347775 | ||||||
| chr1:44347792
|
T | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+5058A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347792 | ||||||
| chr1:44347879
|
T | TTG | 65 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.211+4969_211+4970d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347879 | ||||||
| chr1:44347879
|
T | TTGTG | 8 | a0001c0001t0001g0097a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG00639.hp2 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+4967_211+4970d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347879 | ||||||
| chr1:44347941
|
A | G | 28 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(25): Show | 28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.211+4909T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347941 | ||||||
| chr1:44348261
|
C | A | 5 | a0001c0001t0001g0241a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG00544.hp2 NA18963.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+4589G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348261 | ||||||
| chr1:44348710
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348710 | ||||||
| chr1:44348748
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4102C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348748 | ||||||
| chr1:44348838
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0311 | 2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.211+4012C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348838 | ||||||
| chr1:44348929
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.211+3921C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348929 | ||||||
| chr1:44348939
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.211+3911G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348939 | ||||||
| chr1:44348953
|
A | G | 27 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0127others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.211+3897T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348953 | ||||||
| chr1:44349000
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.211+3850G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349000 | ||||||
| chr1:44349151
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211+3699C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349151 | ||||||
| chr1:44349314
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3536C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349314 | ||||||
| chr1:44349488
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3362A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349488 | ||||||
| chr1:44349552
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+3298G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349552 | ||||||
| chr1:44349569
|
C | T | 29 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0134others(26): Show | 29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.211+3281G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349569 | ||||||
| chr1:44349925
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2925G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349925 | ||||||
| chr1:44349938
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+2912G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349938 | ||||||
| chr1:44350265
|
CT | C | 46 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0126others(43): Show | 46 | HG00438.hp2 HG01884.hp1 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.211+2584delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350265 | ||||||
| chr1:44350331
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0219 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.211+2519C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350331 | ||||||
| chr1:44350730
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+2120A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350730 | ||||||
| chr1:44350743
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.211+2107C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350743 | ||||||
| chr1:44351047
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.211+1803A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351047 | ||||||
| chr1:44351432
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+1418T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351432 | ||||||
| chr1:44351614
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211+1236G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351614 | ||||||
| chr1:44351626
|
G | T | 71 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.211+1224C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351626 | ||||||
| chr1:44351891
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+959A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351891 | ||||||
| chr1:44352093
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+757C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352093 | ||||||
| chr1:44352159
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.211+691G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352159 | ||||||
| chr1:44352369
|
G | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0338others(1): Show | 4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+481C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352369 | ||||||
| chr1:44352405
|
CATAG | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 56 | HG00408.hp1 HG00642.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.211+441_211+444del others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | ||||||
| chr1:44352405
|
CATAGATA others(1): Show |
C | 113 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(110): Show | 113 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.211+437_211+444del others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | ||||||
| chr1:44352405
|
CATAGATA others(5): Show |
C | 139 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(136): Show | 139 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.211+433_211+444del others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | ||||||
| chr1:44352405
|
CATAGATA others(9): Show |
C | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0122others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+429_211+444del others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | ||||||
| chr1:44352405
|
CATAGATA others(13): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.211+425_211+444del others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | ||||||
| chr1:44352453
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211+397C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352453 | ||||||
| chr1:44352462
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211+388T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352462 | ||||||
| chr1:44352529
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.211+321A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352529 | ||||||
| chr1:44352665
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.211+185C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352665 | ||||||
| chr1:44353509
|
T | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.136-584A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353509 | ||||||
| chr1:44353703
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 233 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.136-778T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353703 | ||||||
| chr1:44353885
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-960T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353885 | ||||||
| chr1:44354004
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+888A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354004 | ||||||
| chr1:44354226
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.135+666T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354226 | ||||||
| chr1:44354385
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+507T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354385 | ||||||
| chr1:44354576
|
G | A | 105 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(102): Show | 105 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+316C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354576 | ||||||
| chr1:44354647
|
A | G | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.135+245T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354647 | ||||||
| chr1:44354676
|
C | G | 1 | a0001c0001t0001g0001 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.135+216G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354676 |